Quinoxaline derivatives as pi3 kinase inhibitors

ABSTRACT

Invented is a method of inhibiting the activity/function of PI3 kinases using quinoxaline derivatives. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, allergy, asthma, pancreatitis, multiorgan failure, kidney diseases, platelet aggregation, cancer, sperm motility, transplantation rejection, graft rejection and lung injuries by the administration of quinoxaline derivatives.

FIELD OF THE INVENTION

This invention relates to the use of quinoxaline derivatives for themodulation, notably the inhibition of the activity or function of thephosphoinositide 3′ OH kinase family (hereinafter PI3 kinases),suitably, PI3Kα, PI3δ, PI3Kβ, and/or PI3Kγ. Suitably, the presentinvention relates to the use of quinoxalines in the treatment of one ormore disease states selected from: autoimmune disorders, inflammatorydiseases, cardiovascular diseases, neurodegenerative diseases, allergy,asthma, pancreatitis, multiorgan failure, kidney diseases, plateletaggregation, cancer, sperm motility, transplantation rejection, graftrejection and lung injuries.

BACKGROUND OF THE INVENTION

Cellular membranes represent a large store of second messengers that canbe enlisted in a variety of signal transduction pathways. In regardsfunction and regulation of effector enzymes in phospholipids signalingpathways, these enzymes generate second messengers from the membranephospholipid pools (class I PI3 kinases (e.g. PI3Kalpha)) aredual-specificity kinase enzymes, meaning they display both: lipid kinase(phosphorylation of phosphoinositides) as well as protein kinaseactivity, shown to be capable of phosphorylation of protein assubstrate, including auto-phosphorylation as intramolecular regulatorymechanism. These enzymes of phospholipids signaling are activated inresponse to a variety of extra-cellular signals such as growth factors,mitogens, integrins (cell-cell interactions) hormones, cytokines,viruses and neurotransmitters such as described in Scheme A hereinafterand also by intracellular regulation by other signaling molecules(cross-talk, where the original signal can activate some parallelpathways that in a second step transmit signals to PI3Ks byintra-cellular signaling events), such as small GTPases, kinases orphosphatases for example. Intracellular regulation can also occur as aresult of aberrant expression or lack of expression of cellularoncogenes or tumor suppressors. The inositol phospholipid(phosphoinositides) intracellular signaling pathways begin withactivation of a signaling molecules (extra cellular ligands, stimuli,receptor dimerization, transactivation by heterologous receptor (e.g.receptor tyrosine kinase)) the recruitment and activation of PI3Kincluding the involvement of G-protein linked transmembrane receptorintegrated into the plasma membrane.

PI3K converts the membrane phospholipids PI(4,5)P₂ into PI(3,4,5)P₃ thatfunctions as a second messenger. PI and PI(4)P are also substrates ofPI3K and can be phosphorylated and converted into PI3P and PI(3,4)P₂,respectively. In addition, these phosphoinositides can be converted intoother phosphoinositides by 5′-specific and 3′-specific phophatases, thusPI3K enzymatic activity results either directly or indirectly in thegeneration of two 3′-phosphoinositide subtypes that function as 2^(nd)messengers in intra-cellular signal transduction pathways (TrendsBiochem. Sci. 22(7) p. 267-72 (1997) by Vanhaesebroeck et al.: Chem.Rev. 101(8) p. 2365-80 (2001) by Leslie et al (2001); Annu. Rev. Cell.Dev. Biol. 17p, 615-75 (2001) by Katso et al. and Cell. Mol. Life. Sci.59(5) p. 761-79 (2002) by Toker et al.). Multiple PI3K isoformscategorized by their catalytic subunits, their regulation bycorresponding regulatory subunits, expression patterns andsignaling-specific functions (p110α, β, δ and γ) perform this enzymaticreaction (Exp. Cell. Res. 25 (1) p. 239-54 (1999) by Vanhaesebroeck andKatso et al., 2001, above).

The closely related isoforms p110α and β are ubiquitously expressed,while δ and γ are more specifically expressed in the haematopoietic cellsystem, smooth muscle cells, myocytes and endothelial cells (TrendsBiochem. Sci. 22(7) p. 267-72 (1997) by Vanhaesebroeck et al.). Theirexpression might also be regulated in an inducible manner depending onthe cellular, tissue type and stimuli as well as disease context.Inducibility of protein expression includes synthesis of protein as wellas protein stabilization that is in part regulated by association withregulatory subunits.

To date, eight mammalian PI3Ks have been identified, divided into threemain classes (I, II, and III) on the basis of sequence homology,structure, binding partners, mode of activation, and substratepreference. In vitro, class I PI3Ks can phosphorylatephosphatidylinositol (PI), phosphatidylinositol-4-phosphate (PI4P), andphosphatidylinositol-4,5-bisphosphate (PI(4,5)P₂) to producephosphatidylinositol-3-phosphate (PI3P),phosphatidylinositol-3,4-bisphosphate (PI(3,4)P₂, andphosphatidylinositol-3,4,5-trisphosphate (PI(3,4,5)P₃, respectively.Class II PI3Ks phosphorylate PI and phosphatidylinositol-4-phosphate.Class III PI3Ks can only phosphorylate PI (Vanhaesebrokeck et al., 1997,above; Vanhaesebroeck et al., 1999, above and Leslie et al, 2001, above)

As illustrated in Scheme A above, phosphoinositide 3-kinases (PI3Ks)phosphorylate the hydroxyl of the third carbon of the inositol ring. Thephosphorylation of phosphoinositides that generate PtdIns to3,4,5-trisphosphate (PtdIns(3,4,5)P₃), PtdIns(3,4)P₂ and PtdIns(3)Pproduce second messengers for a variety of signal transduction pathways,including those essential to cell proliferation, cell differentiation,cell growth, cell size, cell survival, apoptosis, adhesion, cellmotility, cell migration, chemotaxis, invasion, cytoskeletalrearrangement, cell shape changes, vesicle trafficking and metabolicpathway (Katso et al., 2001, above and Mol. Med. Today 6(9) p. 347-57(2000) by Stein). G-protein coupled receptors mediated phosphoinositide3′OH-kinase activation via small GTPases such as Gβγ and Ras, andconsequently PI3K signaling plays a central role in establishing andcoordinating cell polarity and dynamic organization of thecytoskeleton—which together provides the driving force of cells to move.

Chemotaxis—the directed movement of cells toward a concentrationgradient of chemical attractants, also called chemokines is involved inmany important diseases such as inflammation/auto-immunity,neurodegeneration, antiogenesis, invasion/metastasis and wound healing(Immunol. Today 21(6) p. 260-4 (2000) by Wyman et al.; Science 287(5455)p. 1049-53 (2000) by Hirsch et al.; FASEB J. 15(11) p. 2019-21 (2001) byHirsch et al. and Nat. Immunol. 2(2) p. 108-15 (2001) by Gerard et al.).

Recent advances using genetic approaches and pharmacological tools haveprovided insights into signalling and molecular pathways that mediatechemotaxis in response to chemoattractant activated G-protein coupledreceptors PI3-Kinase, responsible for generating these phosphorylatedsignalling products, was originally identified as an activity associatedwith viral oncoproteins and growth factor receptor tyrosine kinases thatphosphorylates phosphatidylinositol (PI) and its phosphorylatedderivatives at the 3′-hydroxyl of the inositol ring (Panayotou et al.,Trends Cell Biol. 2 p. 358-60 (1992)). However, more recent biochemicalstudies revealed that, class I PI3 kinases (e.g. class IB isoform PI3Kγ)are dual-specific kinase enzymes, means they display both: lipid kinase(phosphorylation of phospho-inositides) as well as protein kinaseactivity, shown to be capable of phosphorylation of other protein assubstrates, including auto-phosphorylation as intra-molecular regulatorymechanism.

PI3-kinase activation, is therefore believe to be involved in a range ofcellular responses including cell growth, differentiation, and apoptosis(Parker et al., Current Biology, 5 p. 577-99 (1995); Yao et al.,Science, 267 p. 2003-05 (1995)). PI3-kinase appears to be involved in anumber of aspects of leukocyte activation. A p85-associated PI3-kinaseactivity has been shown to physically associate with the cytoplasmicdomain of CD28, which is an important costimulatory molecule for theactivation of T-cells in response to antigen (Pages et al., Nature, 369p. 327-29 (1994); Rudd, Immunity 4 p. 527-34 (1996)). Activation of Tcells through CD28 lowers the threshold for activation by antigen andincreases the magnitude and duration of the proliferative response.These effects are linked to increases in the transcription of a numberof genes including interleukin-2 (IL2), an important T cell growthfactor (Fraser et al., Science 251 p. 313-16 (1991)). Mutation of CD28such that it can longer interact with PI3-kinase leads to a failure toinitiate IL2 production, suggesting a critical role for PI3-kinase in Tcell activation. PI3Kγ has been identified as a mediator of Gbeta-gamma-dependent regulation of JNK activity, and G beta-gamma aresubunits of heterotrimeric G proteins (Lopez-Ilasaca et al., J. Biol.Chem. 273(5) p. 2505-8 (1998)). Cellular processes in which PI3Ks playan essential role include suppression of apoptosis, reorganization ofthe actin skeleton, cardiac myocyte growth, glycogen synthasestimulation by insulin, TNFα-mediated neutrophil priming and superoxidegeneration, and leukocyte migration and adhesion to endothelial cells.

Recently, (Laffargue et al., Immunity 16(3) p. 441-51 (2002)) it hasbeen described that PI3Kγ relays inflammatory signals through variousG(i)-coupled receptors and its central to mast cell function, stimuli incontext of leukocytes, immunology includes cytokines, chemokines,adenosines, antibodies, integrins, aggregation factors, growth factors,viruses or hormones for example (J. Cell. Sci. 114(Pt 16) p. 2903-10(2001) by Lawlor et al.; Laffargue et al., 2002, above and Curr. OpinionCell Biol. 14(2) p. 203-13 (2002) by Stephens et al.).

Specific inhibitors against individual members of a family of enzymesprovide invaluable tools for deciphering functions of each enzyme. Twocompounds, LY294002 and wortmannin (cf. hereinafter), have been widelyused as PI3-kinase inhibitors. These compounds are non-specific PI3Kinhibitors, as they do not distinguish among the four members of Class IPI3-kinases. For example, the IC₅₀ values of wortmannin against each ofthe various Class I PI3-kinases are in the range of 1-10 nM. Similarly,the IC₅₀ values for LY294002 against each of these PI3-kinases is about15-20 μM (Fruman et al., Ann. Rev. Biochem., 67, p. 481-507 (1998)),also 5-10 microM on CK2 protein kinase and some inhibitory activity onphospholipases. Wortmannin is a fungal metabolite which irreversiblyinhibits PI3K activity by binding covalently to the catalytic domain ofthis enzyme. Inhibition of PI3K activity by wortmannin eliminatessubsequent cellular response to the extracellular factor. For example,neutrophils respond to the chemokine fMet-Leu-Phe (fMLP) by stimulatingPI3K and synthesizing PtdIns (3, 4, 5)P₃. This synthesis correlates withactivation of the respirators burst involved in neutrophil destructionof invading microorganisms. Treatment of neutrophils with wortmanninprevents the fMLP-induced respiratory burst response (Thelen et al.,Proc. Natl. Acad. Sci. USA, 91, p. 4960-64 (1994)). Indeed, theseexperiments with wortmannin, as well as other experimental evidence,shows that PI3K activity in cells of hematopoietic lineage, particularlyneutrophils, monocytes, and other types of leukocytes, is involved inmany of the non-memory immune response associated with acute and chronicinflammation.

Based on studies using wortmannin, there is evidence that PI3-kinasefunction is also required for some aspects of leukocyte signalingthrough G-protein coupled receptors (Thelen et al., 1994, above).Moreover, it has been shown that wortmannin and LY294002 blockneutrophil migration and superoxide release. Cyclooxygenase inhibitingbenzofuran derivatives are disclosed by John M. Janusz et al., in J.Med. Chem. 1998; Vol. 41, No. 18.

It is now well understood that deregulation of onocogenes andtumour-suppressor genes contributes to the formation fo malignanttumours, for example by way of increase cell growth and proliferation orincreased cell survival. It is also now known that signaling pathwaysmediated by the PI3K family have a central role in a number of cellprocesses including proliferation and survival, and deregulation ofthese pathways is a causative factor a wide spectrum of human cancersand other diseases (Katso et al., Annual Rev. Cell Dev. Biol., 2001, 17:615-617 and Foster et al., J. Cell Science, 2003, 116: 3037-3040).

Class I PI3K is a heterodimer consisting of a p110 catalytic subunit anda regulatory subunit, and the family is further divided into class Iaand Class Ib enzymes on the basis of regulatory partners and mechanismof regulation. Class Ia enzymes consist of three distinct catalyticsubunits (p110α, p110β, and p110δ) that dimerise with five distinctregulatory subunits (p85α, p55α, p50α, p85β, and p55γ), with allcatalytic subunits being able to interact with all regulatory subunitsto form a variety of heterodimers. Class Ia PI3K are generally activatedin response to growth factor-stimulation of receptor tyrosine kinases,via interaction of the regulatory subunit SH2 domains with specificphospho-tyrosine residues of the activated receptor or adaptor proteinssuch as IRS-1. Small GTPases (ras as an example) are also involved inthe activation of PI3K in conjunction with receptor tyrosine kinaseactivation. Both p110α and p110β are constitutively expressed in allcell types, whereas p110δ expression is more restricted to leukocytepopulations and some epithelial cells. In contrast, the single Class Ibenzyme consists of a p110γ catalytic subunit that interacts with a p101regulatory subunit. Furthermore, the Class Ib enzyme is activated inresponse to G-protein coupled receptor (GPCR) systems and its expressionappears to be limited to leukocytes.

There is now considerable evidence indicating that Class Ia PI3K enzymescontribute to tumourigenesis in a wide variety of human cancers, eitherdirectly or indirectly (Vivanco and Sawyers, Nature Reviews Cancer,2002, 2, 489-501). For example, the p110α subunit is amplified in sometumours such as those of the ovary (Shayesteh, et al., Nature Genetics,1999, 21: 99-102) and cervix (Ma et al., Oncogene, 2000, 19: 2739-2744).More recently, activating mutations within p110α (PIK3CA gene) have beenassociated with various other tumors such as those of the colon and ofthe breast and lung (Samuels, et al., Science, 2004, 304, 554).Tumor-related mutations in p85α have also been identified in cancerssuch as those of the ovary and colon (Philp et al., Cancer Research,2001, 61, 7426-7429). In addition to direct effects, it is believed thatactivation of Class Ia PI3K contributes to tumourigenic events thatoccur upstream in signaling pathways, for example by way ofligand-dependent or ligand-independent activation of receptor tyrosinekinases, GPCR systems or integrins (Vara et al., Cancer TreatmentReviews, 2004, 30, 193-204). Examples of such upstream signalingpathways include over-expression of the receptor tyrosine kinase Erb2 ina variety of tumors leading to activation of PI3K-mediated pathways(Harari et al., Oncogene, 2000, 19, 6102-6114) and over-expression ofthe oncogene Ras (Kauffmann-Zeh et al., Nature, 1997, 385, 544-548). Inaddition, Class Ia PI3Ks may contribute indirectly to tumourigenesiscaused by various downstream signaling events. For example, loss offunction of the PTEN tumor-suppressor phosphatase that catalysesconversion of PI(3,4,5)P3 back to PI(4,5)P2 is associated with a verybroad range of tumors via deregulation of PI3K-mediated production ofPI(3,4,5)P3 (Simpson and Parsons, Exp. Cell Res., 2001, 264, 29-41).Furthermore, augmentation of the effects of other PI3K-mediatedsignaling events is believed to contribute to a variety of cancers, forexample by activation of AKT (Nicholson and Andeson, Cellular Signaling,2002, 14, 381-395).

In addition to a role in mediating proliferative and survival signalingin tumor cells, there is also good evidence that class Ia PI3K enzymesalso contributes to tumourigenesis via its function in tumor-associatedstromal cells. For examples, PI3K signaling is known to play animportant role in mediating angiogenic events in endothelial cells inresponse to pro-angiogenic factors such as VEGF (abid et al.,Arterioscler, Thromb. Vasc. Biol., 2004, 24, 294-300). As Class I PI3Kenzymes are also involved in motility and migration (Sawyer, ExpertOpinion investing. Drugs, 2004, 13, 1-19), PI3K inhibitors areanticipated to provide therapeutic benefit via inhibition of tumor cellinvasion and metastasis.

SUMMARY OF THE INVENTION

This invention relates to novel compounds of Formula (I):

-   -   in which    -   R1 is an optionally substituted ring system selected from a        group consisting of: formula (II), (III), (IV), (V), (VI), (VII)        and (VIII):

-   -   each R2, R3 and R4 is independently selected from: hydrogen,        halogen, acyl, amino, substituted amino, arylamino, acylamino,        heterocycloalkylamino, C1-6alkyl, substituted C1-6alkyl,        C3-7cycloalkyl, substituted C3-7cycloalkyl,        C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl,        alkylcarboxy, aminoalkyl, aryl, substituted aryl, heteroaryl,        substituted heteroaryl, arylalkyl, substituted arylalkyl,        arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl,        substituted heteroarylalkyl, cyano, hydroxyl, alkoxy, acyloxy,        and aryloxy;    -   n is 0-2;    -   X is C or N; Y is C, O, N or S;    -   and/or a pharmaceutically acceptable salt, hydrate, solvate or        pro-drug thereof;    -   provided that in each of formula (V) to (VIII) at least one Y is        not carbon;    -   further provided that formula (VIII) is substituted with at        least one oxo group;    -   further provided that when R1 is imidazolidinedione or        4-pyridinyl R2 is not substituted aryl, thienyl or substituted        thienyl.

Suitably, the invention relates to a compound of formula (I) or apharmaceutically acceptable salt thereof.

This invention also relates to a method of treating cancer, whichcomprises administering to a subject in need thereof an effective amountof a compound of Formula (I).

This invention also relates to a method of treating one or more diseasestates selected from: autoimmune disorders, inflammatory diseases,cardiovascular diseases, neurodegenerative diseases, allergy, asthma,pancreatitis, multiorgan failure, kidney diseases, platelet aggregation,sperm motility, transplantation rejection, graft rejection and lunginjuries, which comprises administering to a subject in need thereof aneffective amount of a compound of Formula (I).

Included in the present invention are methods of co-administering thepresent PI3 kinase inhibiting compounds with further active ingredients.

DETAILED DESCRIPTION OF THE INVENTION

This invention relates to novel compounds of Formula (I) as describedabove.

Suitably, this invention relates to novel compounds of Formula (I)(A):

-   -   in which    -   R1 is an optionally substituted ring system selected from a        group consisting of: formula (II), (III), (IV), (V), (VI), (VII)        and (VIII):

-   -   each R3 and R4 is independently selected from a group consisting        of: hydrogen, halogen, acyl, amino, substituted amino,        C1-6alkyl, substituted C1-6alkyl, C3-7cycloalkyl, substituted        C3-7cycloalkyl, C3-7heterocycloalkyl, substituted        C3-7heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl,        substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl,        substituted arylalkyl, arylcycloalkyl, substituted        arylcycloalkyl, heteroarylalkyl, substituted heteroarylalkyl,        cyano, hydroxyl, alkoxy, acyloxy, and aryloxy;    -   R2 is selected from a group consisting of: aryl, heteroaryl,        substituted heteroaryl, substituted aryl, heterocycloalkyl,        substituted heterocycloalkyl, amino, substituted amino,        arylamino, acylamino, heterocycloalkylamino, hydroxyl, alkoxy;    -   n is 0-2;    -   X is C or N; Y is C, O, N or S;    -   and/or a pharmaceutically acceptable salt, hydrate, solvate or        pro-drug thereof;    -   provided that in each of formula (V) to (VIII) at least one Y is        not carbon;    -   further provided that formula (VIII) is substituted with at        least one oxo group;    -   further provided that R1 is not imidazolidinedione, and when R1        is 4-pyridinyl R2 is not aryl, substituted aryl, thienyl or        substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(B):

-   -   in which    -   R1 is an optionally substituted ring system selected from a        group consisting of: formula (II), (III), (IV), (V), (VI), (VII)        and (VIII):

-   -   each R3 and R4 is independently selected from a group consisting        of: hydrogen, halogen, acyl, amino, substituted amino,        C1-6alkyl, substituted C1-6alkyl, C3-7cycloalkyl, substituted        C3-7cycloalkyl, C3-7heterocycloalkyl, substituted        C3-7heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl,        substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl,        substituted arylalkyl, arylcycloalkyl, substituted        arylcycloalkyl, heteroarylalkyl, substituted heteroarylalkyl,        cyano, hydroxyl, alkoxy, acyloxy, and aryloxy;    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, hydroxyl, alkyl, substituted        alkyl;    -   n is 0-2;    -   X is C or N; Y is C, O, N or S;    -   and/or a pharmaceutically acceptable salt, hydrate, solvate or        pro-drug thereof;    -   provided that in each of formula (V) to (VIII) at least one Y is        not carbon;    -   further provided that formula (VIII) is substituted with at        least one oxo group;    -   further provided that R1 is not imidazolidinedione, R2 is not        thienyl or substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(C):

-   -   in which    -   R1 is an optionally substituted ring system selected from a        group consisting of: formula (II), (III), and (IV) as defined        above;    -   R3 and R4 are hydrogens;    -   R2 is selected from a group consisting of: aryl, substituted        aryl, heteroaryl, substituted heteroaryl, heterocycloalkyl,        substituted heterocycloalkyl, amino, substituted amino,        arylamino, acylamino, heterocycloalkylamino, hydroxyl, alkoxy;    -   n is 0-2;    -   X is C or N; Y is C, O, N or S;    -   and/or a pharmaceutically acceptable salt, hydrate, solvate or        pro-drug thereof;    -   provided that R1 is not imidazolidinedione and when R1 is        4-pyridine R2 is not aryl, substituted aryl, thienyl or        substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(D):

-   -   in which    -   R1 is an optionally substituted ring system selected from a        group consisting of: formula (II), (III), and (IV) as defined        above;    -   R3 and R4 are hydrogens;    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, hydroxyl;    -   n is 0-2;    -   X is C or N; Y is C, O, N or S;    -   and/or a pharmaceutically acceptable salt, hydrate, solvate or        pro-drug thereof;    -   provided that R1 is not imidazolidinedione and R2 is not thienyl        or substituted thienyl.

Suitably, this invention relates to compounds of formula (I)(A), whereinR1 is an optionally substituted six-membered heteroaryl ring containingat least one nitrogen.

Suitably, this invention relates to novel compounds of Formula (I)(E):

-   -   in which    -   R1 is an optionally substituted ring system selected from a        group consisting of: formula (II), (III), and (IV) as defined        above;    -   R4 is hydrogen;    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, arylamino, acylamino,        heterocycloalkylamino, substituted amino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   n is 0;    -   X is C or N;    -   or a pharmaceutically acceptable salt thereof;    -   provided that R2 is not thienyl or substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(F):

-   -   in which    -   R1 is an optionally substituted pyridinyl ring;    -   R4 is hydrogen;    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   n is 0;    -   or a pharmaceutically acceptable salt thereof;    -   provided that R2 is not thienyl or substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(G):

-   -   in which    -   each R2, R3, R4 and R5 is independently selected from: hydrogen,        halogen, acyl, amino, substituted amino, arylamino, acylamino,        heterocycloalkylamino, C1-6alkyl, substituted C1-6alkyl,        C3-7cycloalkyl, substituted C3-7cycloalkyl,        C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl,        alkylcarboxy, aminoalkyl, aryl, substituted aryl, heteroaryl,        substituted heteroaryl, arylalkyl, substituted arylalkyl,        arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl,        substituted heteroarylalkyl, cyano, hydroxyl, alkoxy, acyloxy,        and aryloxy;    -   or R5 is R6, wherein R6 is —SO2NR80 or —NSO₂R80, in which R80 is        selected from a group consisting of: C1-C6alkyl,        C1-C6cycloalkyl, C1-C6heterocycloalkyl, substituted C1-C6alkyl,        substituted C1-C6cycloalkyl, substituted C1-C6heterocycloalkyl,        aryl optionally fused with a five-membered ring or substituted        with one to five groups selected from a group consisting of:        C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH,    -   n is 0-2, m is 0-3;    -   or a pharmaceutically acceptable salt thereof;    -   provided that R2 is not thienyl or substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(H):

-   -   in which    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   each R3 and R4 is independently selected from: hydrogen,        halogen, acyl, amino, substituted amino, C1-6alkyl, substituted        C1-6alkyl, C3-7cycloalkyl, substituted C3-7cycloalkyl,        C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl, cyano,        hydroxyl and alkoxy;    -   each R5 is independently selected from: hydrogen, halogen, acyl,        amino, substituted amino, C1-6alkyl, substituted C1-6alkyl,        C3-7cycloalkyl, substituted C3-7cycloalkyl,        C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl, cyano,        hydroxyl and alkoxy; or R5 is R6, wherein R6 is —SO2NR80 or        —NSO₂R80, in which R80 is selected from a group consisting of:        C1-C6alkyl, C1-C6cycloalkyl, C1-C6heterocycloalkyl, substituted        C1-C6alkyl, substituted C1-C6cycloalkyl, substituted        C1-C6heterocycloalkyl, aryl optionally fused with a        five-membered ring or substituted with one to five groups        selected from a group consisting of: C1-C6alkyl,        C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH;    -   n is 0-2, m is 0-2;    -   or a pharmaceutically acceptable salt thereof;    -   provided that R2 is not thienyl or substituted thienyl.

Suitably, this invention relates to novel compounds of Formula (I)(J):

-   -   in which    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   each R3 and R4 is independently selected from: hydrogen,        halogen, acyl, amino, substituted amino, C1-6alkyl, substituted        C1-6alkyl, C3-7cycloalkyl, substituted C3-7cycloalkyl,        C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl, cyano,        hydroxyl and alkoxy;    -   each R5 is independently selected from: hydrogen, halogen, acyl,        amino, substituted amino, C1-6alkyl, substituted C1-6alkyl,        C3-7cycloalkyl, substituted C3-7cycloalkyl,        C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl, cyano,        hydroxyl, alkoxy, nitro;    -   R6 is —SO₂NR80 or —NSO₂R80, in which R80 is selected from a        group consisting of: C1-C6alkyl, C1-C6cycloalkyl,        C1-C6heterocycloalkyl, substituted C1-C6alkyl, substituted        C1-C6cycloalkyl, substituted C1-C6heterocycloalkyl, aryl        optionally fused with a five-membered ring or substituted with        one to five groups selected from a group consisting of:        C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH;    -   n is 0-2, m is 0-2;    -   or a pharmaceutically acceptable salt thereof.

Suitably, this invention relates to novel compounds of Formula (I)(K):

-   -   in which    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   R4 is hydrogen;    -   each R5 is independently selected from: hydrogen, halogen, acyl,        amino, substituted amino, C1-6alkyl, substituted C1-6alkyl,        cyano, hydroxyl, alkoxy;    -   n is 0, m is 0-1;    -   R6 is —SO₂NR80 or —NSO₂R80, in which R80 is selected from a        group consisting of: C1-C6alkyl, C1-C6cycloalkyl,        C1-C6heterocycloalkyl, substituted C1-C6alkyl, substituted        C1-C6cycloalkyl, substituted C1-C6heterocycloalkyl, aryl        optionally fused with a five-membered ring or substituted with        one to five groups selected from a group consisting of:        C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH, wherein n is 0-2;    -   or a pharmaceutically acceptable salt thereof.

Suitably, this invention relates to novel compounds of Formula (I)(L):

-   -   in which    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   each R5 is independently selected from: hydrogen, halogen, acyl,        amino, substituted amino, C1-6alkyl, substituted C1-6alkyl,        cyano, hydroxyl, alkoxy;    -   m is 0-1;    -   R6 is —SO₂NR80 or —NSO₂R80, wherein R80 is selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl,        C1-C6heterocycloalkyl, substituted C1-C6alkyl, substituted        C1-C6cycloalkyl, substituted C1-C6heterocycloalkyl, aryl        optionally fused with a five-membered ring or substituted with        one to five groups selected from a group consisting of:        C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH;    -   or a pharmaceutically acceptable salt thereof.

Suitably, this invention relates to novel compounds of Formula (I)(M):

-   -   in which    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   each R5 is independently selected from: hydrogen, halogen, acyl,        amino, substituted amino, C1-6alkyl, substituted C1-6alkyl,        cyano, hydroxyl, alkoxy;    -   m is 0-1;    -   R6 is —NSO₂R80, wherein R80 is selected from a group consisting        of: C1-C6alkyl, C1-C6cycloalkyl, C1-C6heterocycloalkyl,        substituted C1-C6alkyl, substituted C1-C6cycloalkyl, substituted        C1-C6heterocycloalkyl, aryl optionally fused with a        five-membered ring or substituted with one to five groups        selected from a group consisting of: C1-C6alkyl,        C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH, wherein n is 0-2;    -   or a pharmaceutically acceptable salt thereof.

Suitably, this invention relates to novel compounds of Formula (I)(N):

-   -   in which    -   R2 is selected from a group consisting of: heteroaryl,        substituted heteroaryl, heterocycloalkyl, substituted        heterocycloalkyl, amino, substituted amino, arylamino,        acylamino, heterocycloalkylamino, alkoxy, C1-6alkyl and        substituted C1-6alkyl;    -   each R5 is independently selected from: hydrogen, halogen, acyl,        amino, substituted amino, C1-6alkyl, substituted C1-6alkyl,        cyano, hydroxyl, alkoxy;    -   m is 0-1;    -   R6 is —SO₂NR80, wherein R80 is selected from a group consisting        of: C1-C6alkyl, C1-C6cycloalkyl, C1-C6heterocycloalkyl,        substituted C1-C6alkyl, substituted C1-C6cycloalkyl, substituted        C1-C6heterocycloalkyl, aryl optionally fused with a        five-membered ring or substituted with one to five groups        selected from a group consisting of: C1-C6alkyl,        C1-C6cycloalkyl, halogen, amino, substituted amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH,        or heteroaryl optionally fused with a five-membered ring or        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or        —(CH₂)_(n)COOH, wherein n is 0-2;    -   or a pharmaceutically acceptable salt thereof.

Suitably, this invention relates to compounds of Formulas (I)M) and(I)(N), wherein

-   -   R2 is selected from the group consisting of: optionally        substituted piperazine, optionally substituted pyrazole,        substituted amino and optionally substituted piperidine;    -   R80 is selected from a group consisting of: C1-C6alkyl,        C1-C6cycloalkyl, C1-C6heterocycloalkyl, substituted C1-C6alkyl,        substituted C1-C6cycloalkyl, substituted C1-C6heterocycloalkyl,        aryl and substituted aryl.

Suitably, this invention relates to compounds of Formulas (I)M) and(I)(N), wherein

-   -   R2 is selected from the group consisting of: optionally        substituted piperazine, optionally substituted pyrazole,        substituted amino and optionally substituted piperidine;    -   R80 is selected from a group consisting of: aryl optionally        substituted with one to five groups selected from a group        consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,        substituted amino, trifluoromethyl, cyano, hydroxyl, alkoxy, oxo        or —(CH₂)_(n)COOH, or heteroaryl optionally substituted with one        to five groups selected from a group consisting of: C1-C6alkyl,        C1-C6cycloalkyl, halogen, amino, trifluoromethyl, cyano,        hydroxyl, alkoxy, oxo, or —(CH₂)_(n)COOH, wherein n is 0-2.

Suitably, this invention relates to the following compounds:

-   5-[3-(4-pyridinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   2-amino-N,N-dimethyl-5-[3-(4-pyridinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-[3-(3-pyridinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-(3-phenyl-6-quinoxalinyl)-3-pyridinesulfonamide;-   7-[6-(methyloxy)-3-pyridinyl]-2-(4-morpholinyl)quinoxaline;-   2-(4-morpholinyl)-7-[4-(4-pyridinyl)-6-quinolinyl]quinoxaline;-   2-(4-morpholinyl)-7-(1H-pyrrolo[2,3-b]pyridin-5-yl)quinoxaline;-   7-(1H-indazol-5-yl)-2-(4-morpholinyl)quinoxaline;-   2-(4-morpholinyl)-7-(4-pyridinyl)quinoxaline;-   2-(4-morpholinyl)-7-(3-pyridinyl)quinoxaline;-   7-[2-(methyloxy)-3-pyridinyl]-2-(4-morpholinyl)quinoxaline;-   7-(1H-pyrrolo[2,3-b]pyridin-5-yl)-2(1H)-quinoxalinone;-   ethyl    1-[7-(1H-pyrrolo[2,3-b]pyridin-5-yl)-2-quinoxalinyl]-3-piperidinecarboxylate;-   2-(4-morpholinyl)-7-(1H-pyrazolo[3,4-b]pyridin-5-yl)quinoxaline;-   2-(4-pyridinyl)-7-(1H-pyrrolo[2,3-b]pyridin-5-yl)quinoxaline;-   2-amino-N,N-dimethyl-5-[3-(4-morpholinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   2-(4-morpholinyl)-7-[5-(4-morpholinylsulfonyl)-3-pyridinyl]quinoxaline;-   5-[3-(4-morpholinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   2-amino-N,N-dimethyl-5-(3-oxo-3,4-dihydro-6-quinoxalinyl)-3-pyridinesulfonamide;-   2-amino-N,N-dimethyl-5-(3-{[2-(4-morpholinyl)ethyl]amino}-6-quinoxalinyl)-3-pyridinesulfonamide;-   2-amino-5-{3-[[2-(dimethylamino)ethyl](methyl)amino]-6-quinoxalinyl}N,N-dimethyl-3-pyridinesulfonamide;-   2-amino-N,N-dimethyl-5-(3-{[2-(methyloxy)ethyl]amino}-6-quinoxalinyl)-3-pyridinesulfonamide;-   2-amino-5-{7-[6-(methyloxy)-3-pyridinyl]-2-quinoxalinyl}-3-pyridinesulfonamide;-   2-amino-5-{3-[(2-hydroxyethyl)(methyl)amino]-6-quinoxalinyl}-N,N-dimethyl-3-pyridinesulfonamide;-   2-amino-5-[3-(ethylamino)-6-quinoxalinyl]-N,N-dimethyl-3-pyridinesulfonamide;-   2-amino-N,N-dimethyl-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-(3-{[2-(2-pyridinyl)ethyl]amino}-6-quinoxalinyl)-3-pyridinesulfonamide;-   5-{3-[4-(methylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-[3-(1-piperidinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-[3-(4-hydroxy-1-piperidinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-[3-(2,6-dimethyl-4-morpholinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   1,1-dimethylethyl    4-{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}-1-piperazinecarboxylate;-   5-{3-[(2,2-dimethylpropyl)amino]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   1,1-dimethylethyl    {2-[{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}(methyl)amino]ethyl}carbamate;-   5-[3-(4-acetyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-{3-[4-(2-hydroxyethyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-{3-[4-(2-furanylcarbonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-(3-{4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   5-{3-[4-(2-methylpropanoyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-{3-[(1,1-dimethylethyl)amino]-6-quinoxalinyl}-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-{3-[4-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   N-{2-chloro-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[4-(methylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)methanesulfonamide;-   N-{5-[3-(4-morpholinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   2-methyl-N-(5-{3-[4-(methylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-(2,4-difluorophenyl)-5-[3-(4-morpholinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   3-{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}-N-methylbenzamide;-   5-(3-{3-[(methylamino)sulfonyl]phenyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   5-[3-(1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-[3-(1H-pyrazol-3-yl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   N-{2-chloro-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(2,4-difluorophenyl)-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinamine;-   N-{2-methyl-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(2,4-difluorophenyl)-5-(3-{1-[2-(dimethylamino)ethyl]-1H-pyrazol-4-yl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   2,4-difluoro-N-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(3-furanyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{2-chloro-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}-2,4-difluorobenzenesulfonamide;-   2,4-difluoro-N-{2-methyl-5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[5-(3-{1-[2-(dimethylamino)ethyl]-1H-pyrazol-4-yl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(1-ethyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-5-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1,3,5-trimethyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(3,5-dimethyl-4-isoxazolyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[1-(2-methylpropyl)-1H-pyrazol-4-yl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[5-(3-{1-[2-(4-morpholinyl)ethyl]-1H-pyrazol-4-yl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-(5-{3-[1-(phenylsulfonyl)-1H-pyrazol-4-yl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{5-[3-(1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   [4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1H-pyrazol-1-yl]acetic    acid;-   N-{5-[3-(1-methyl-1H-pyrazol-3-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N,N-dimethyl-2-[4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1H-pyrazol-1-yl]acetamide;-   N-[5-(3-imidazo[1,2-a]pyridin-3-yl-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   2-[4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1H-pyrazol-1-yl]acetamide;-   N-methyl-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N,N-dimethyl-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)benzamide;-   2-phenyl-N-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)acetamide;-   N-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)benzenesulfonamide;-   5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinamine;-   2-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1-phenylmethanesulfonamide;-   N-{2-chloro-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   N-{2-chloro-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2,4-difluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-2-propanesulfonamide;-   1-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-imidazole-4-sulfonamide;-   3-fluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   methyl    4-(methyloxy)-3-[({5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}amino)sulfonyl]benzoate;-   4-cyano-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}methanesulfonamide;-   1-ethyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-pyrazole-4-sulfonamide;-   1,3-dimethyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-pyrazole-4-sulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   1-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-pyrazole-3-sulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1-propanesulfonamide;-   1-cyclohexyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}methanesulfonamide;-   4-fluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-3-(trifluoromethyl)benzenesulfonamide;-   2,2,2-trifluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}ethanesulfonamide;-   3,5-dimethyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-isoxazolesulfonamide;-   1,3,5-trimethyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-pyrazole-4-sulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}ethanesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1-butanesulfonamide;-   4-fluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-(methyloxy)-3-[({5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}amino)sulfonyl]benzoic    acid;-   2-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1-propanesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-2-thiophenesulfonamide;-   2-(methyloxy)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2-fluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   3,4-bis(methyloxy)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2,5-dimethyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-(1-methylethyl)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-propylbenzenesulfonamide;-   4-(methyloxy)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2,5-bis(methyloxy)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-3-(trifluoromethyl)benzenesulfonamide;-   1-cyclopentyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}methanesulfonamide;-   3-fluoro-4-(methyloxy)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-fluoro-2-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2-fluoro-4-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-2-(trifluoromethyl)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(trifluoromethyl)benzenesulfonamide;-   2-chloro-4-fluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2,5-dichloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2,3-dichloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-3-thiophenesulfonamide;-   3-chloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   3-(methyloxy)-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   5-chloro-1,3-dimethyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-pyrazole-4-sulfonamide;-   4-[(4-fluorophenyl)oxy]-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2-chloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-5-(trifluoromethyl)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(4-pyridinyloxy)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(3-pyridinyloxy)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-[(phenylmethyl)oxy]benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(1,3-oxazol-5-yl)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(methylsulfonyl)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(phenyloxy)benzenesulfonamide;-   4′-chloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-biphenylsulfonamide;-   4-{[(2-chloro-1,3-thiazol-5-yl)methyl]oxy}-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-{[2-(methyloxy)phenyl]oxy}-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(2-oxo-1-pyrrolidinyl)benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-(2-methyl-1,3-thiazol-4-yl)benzenesulfonamide;-   N-{2-(ethyloxy)-5-[({5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}amino)sulfonyl]phenyl}-4-morpholinecarboxamide;-   N-{2-(ethyloxy)-5-[({5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}amino)sulfonyl]phenyl}-1-pyrrolidinecarboxamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-2,3-dihydro-1,4-benzodioxin-6-sulfonamide;-   N-{3-methyl-4-[({5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}amino)sulfonyl]phenyl}-4-morpholinecarboxamide;-   4-chloro-N-{4-(ethyloxy)-3-[({5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}amino)sulfonyl]phenyl}benzamide;-   2,6-difluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-2-butanesulfonamide;-   2-chloro-6-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   2-chloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-chloro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-2,1,3-benzoxadiazole-4-sulfonamide;-   N-{2-(methyloxy)-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-methyl-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-3,4-dihydro-2H-1,4-benzoxazine-7-sulfonamide;-   2-amino-N,N-dimethyl-5-[3-(4-pyridinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   3,3′-di-4-morpholinyl-6,6′-biquinoxaline;-   N,N-dimethyl-N′-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}sulfamide;-   N-{2-(methyloxy)-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   2,4-difluoro-N-{2-(methyloxy)-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{2-(methyloxy)-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}methanesulfonamide;-   2,4-difluoro-N-{2-methyl-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{2-methyl-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   1-ethyl-N-{2-(methyloxy)-5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-1H-pyrazole-4-sulfonamide;-   N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-morpholinesulfonamide;-   1,1-dimethylethyl[2-(4-{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}-1-piperazinyl)ethyl]carbamate;-   5-(3-{[2-(dimethylamino)ethyl]oxy}-6-quinoxalinyl)-3-pyridinesulfonamide;-   5-{3-[[3-(dimethylamino)propyl](methyl)amino]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-(3-{4-[3-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   5-{3-[4-(4-acetylphenyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-[3-(4-phenyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinesulfonamide;-   5-(3-{4-[4-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   5-(3-{4-[2-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-(3-{4-[3-(4-morpholinyl)-4-nitrophenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-{3-[4-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-[3-(dimethylamino)-6-quinoxalinyl]-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-{3-[methyl(phenyl)amino]-6-quinoxalinyl}-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-[3-(phenyloxy)-6-quinoxalinyl]-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-(3-{4-[(1-methyl-1H-pyrazol-4-yl)methyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-{3-[4-(3-pyridinylmethyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   N-(2,4-difluorophenyl)-5-{3-[4-(4-pyridinylmethyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinesulfonamide;-   N-{2-chloro-5-[3-(phenylamino)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(2-chloro-5-{3-[3-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-(2-chloro-5-{3-[3-(hydroxymethyl)-1-pyrrolidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-(2-chloro-5-{3-[4-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[2-chloro-5-(3-{4-[(dimethylamino)methyl]-1-piperidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-(2-chloro-5-{3-[3-(dimethylamino)-1-pyrrolidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-(5-{3-[4-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{2-chloro-5-[3-(4-oxo-1-piperidinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[2-chloro-5-(3-{4-[[2-(dimethylamino)ethyl](methyl)amino]-1-piperidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{2-chloro-5-[3-(4-phenyl-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[4-(4-acetylphenyl)-1-piperazinyl]-6-quinoxalinyl}-2-chloro-3-pyridinyl)benzenesulfonamide;-   N-[2-chloro-5-(3-{4-[4-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(4-acetyl-1-piperazinyl)-6-quinoxalinyl]-2-chloro-3-pyridinyl}benzenesulfonamide;-   N-{2-chloro-5-[3-(3-oxo-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   1,1-dimethylethyl    4-(7-{6-chloro-5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate;-   N-{2-chloro-5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-morpholinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(2-chloro-5-{3-[4-(methylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[5-(3-{4-[2-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{3-[4-(methyloxy)phenyl]-1-pyrrolidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{4-[3-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{3-[3-(methyloxy)phenyl]-1-pyrrolidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(4-oxo-1-piperidinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[5-(3-{4-[4-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(4-{[4-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-{[4-(methyloxy)phenyl]carbonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[4-(4-methyl-1-piperazinyl)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-(2-chloro-5-{3-[3-(hydroxymethyl)-1-pyrrolidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-(2-chloro-5-{3-[3-(hydroxymethyl)-1-pyrrolidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   (3Z)-N-(5-{3-[(1-methyl-1H-pyrazol-3-yl)amino]-6-quinoxalinyl}-3-pyridinyl)-1,3-pentadiene-2-sulfonamide;-   N-(5-{3-[(1-methyl-1H-pyrazol-5-yl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[5-(3-{[(1-methyl-1H-pyrazol-4-yl)methyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-(5-{3-[4-(methylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{5-[3-(4-{[2-(methylsulfonyl)ethyl]amino}-1-piperidinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   1,1-dimethylethyl    4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate;-   N-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[5-(3-{3-[3-(methyloxy)phenyl]-1-pyrrolidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{3-[3-(methyloxy)phenyl]-1-pyrrolidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{3-[4-(methyloxy)phenyl]-1-pyrrolidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{3-[4-(methyloxy)phenyl]-1-pyrrolidinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{4-[(2-methylpropyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(2-furanyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(2-thienyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1-methyl-1H-imidazol-5-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(1,3-oxazol-2-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{2-chloro-5-[3-(4-{[4-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-{[4-(methylsulfonyl)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   4-{[4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinyl]sulfonyl}benzenesulfonamide;-   N,N-dimethyl-4-{[4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinyl]sulfonyl}benzenesulfonamide;-   N-[5-(3-{4-[(4-hydroxyphenyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-(5-{3-[4-(4-morpholinylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[5-(3-{4-[(4-acetylphenyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{4-[(4-aminophenyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-{4-[(4-{[(dimethylamino)carbonyl]amino}phenyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   4-{[4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinyl]sulfonyl}benzoic    acid;-   3-[(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)amino]benzoic    acid;-   N-[5-(3-{[3-(methyloxy)phenyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-[5-(3-phenyl-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(1,3-thiazol-5-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[1-(phenylmethyl)-1H-pyrazol-4-yl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[5-(3-{4-[(1-methyl-1H-pyrazol-4-yl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-(5-{3-[4-(cyclohexylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N,N-dimethyl-4-{7-[5-({methylidene[(2Z)-1-methylidene-2,4-pentadien-1-yl]oxido-λ⁴-sulfanyl}amino)-3-pyridinyl]-2-quinoxalinyl}-1-piperazinesulfonamide;-   (2E,4Z)-N-(5-{3-[4-(4-morpholinyl)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)-2,4-hexadiene-3-sulfonamide;-   (3Z)-N-[5-(3-{4-[[2-(dimethylamino)ethyl](methyl)amino]-1-piperidinyl}-6-quinoxalinyl)-3-pyridinyl]-1,3-pentadiene-2-sulfonamide;-   N-(5-{3-[4-(cyclopropylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{5-[3-(4-{[4-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   N-{5-[3-(4-{[4-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-2-oxo-1,2-dihydro-3-pyridinyl}benzenesulfonamide;-   3-(methyloxy)-5-[(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)amino]benzoic    acid;-   N-{5-[3-(4-{[3-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-{[4-(1H-tetrazol-5-yl)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   phenylmethyl    4-[(4-{7-[(1E,2E)-1-ethylidene-3-({[(2Z)-1-methylidene-2,4-pentadien-1-yl]thio}amino)-2-buten-1-yl]-2-quinoxalinyl}-1-piperazinyl)sulfonyl]-1-piperidinecarboxylate;-   1,1-dimethylethyl    4-[7-(5-{[methylidene(oxido)phenyl-□⁴-sulfanyl]amino}-3-pyridinyl)-2-quinoxalinyl]-3-oxo-1-piperazinecarboxylate;-   N-{5-[3-(2-oxo-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-methyl-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinesulfonamide;-   1-{7-[5-({[(1E,3Z)-1-ethenyl-1,3-pentadien-1-yl]sulfonyl}amino)-3-pyridinyl]-2-quinoxalinyl}-4-piperidinesulfonamide;-   1-[7-(5-{[(2Z)-2-buten-1-yl(methylidene)oxido-λ⁴-sulfanyl]amino}-3-pyridinyl)-2-quinoxalinyl]-N,N-dimethyl-4-piperidinesulfonamide;-   (2E,4Z)-N-(5-{3-[4-(methylsulfonyl)-2-oxo-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)-2,4,6-heptatriene-3-sulfonamide;-   N-{5-[3-(4-{[4-(methyloxy)phenyl]sulfonyl}-2-oxo-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N,N′-(2,7-quinoxalinediyldi-5,3-pyridinediyl)dibenzenesulfonamide;-   7-(5-{[(2Z)-2-buten-1-yl(methylidene)-λ⁴-sulfanyl]amino}-3-pyridinyl)-N-phenyl-2-quinoxalinamine;-   N-{5-[3-(4-{[5-{[(dimethylamino)carbonyl]amino}-2-(ethyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N-(2-hydroxyethyl)-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N-(2-hydroxyethyl)-1-{7-[5-(methylamino)-3-pyridinyl]-2-quinoxalinyl}-4-piperidinesulfonamide-1-propene    (1:1);-   N-{5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide;-   7-(5-{[cyclopropyl(methylidene)oxido-λ⁴-sulfanyl]amino}-6-methyl-3-pyridinyl)-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxaline;-   N-{2-(methyloxy)-5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}methanesulfonamide;-   N,N-dimethyl-N′-{5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}sulfamide;-   N-[2-(methyloxy)ethyl]-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N-[4-(aminosulfonyl)phenyl]-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N-[2-(dimethylamino)ethyl]-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinecarboxamide;-   N-{5-[3-(4-{[4-(methyloxy)phenyl]oxy}-1-piperidinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   methyl    2-(methyloxy)-4-[(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)amino]benzoate;-   1,1-dimethylethyl    4-{[1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinyl]carbonyl}-1-piperazinecarboxylate;-   2-amino-N,N-dimethyl-5-{3-[(phenylmethyl)oxy]-6-quinoxalinyl}-3-pyridinesulfonamide;-   5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinamine;-   N-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinyl}acetamide;-   5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinecarbonitrile;-   N-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinyl}methanesulfonamide;-   N-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinyl}-N-(methylsulfonyl)methanesulfonamide;-   2-(4-methyl-1-piperazinyl)-7-[6-(4-morpholinyl)-3-pyridinyl]quinoxaline;-   2-(4-methyl-1-piperazinyl)-7-[6-(1-piperazinyl)-3-pyridinyl]quinoxaline;-   N-{5-[3-(1,1-dioxido-4-thiomorpholinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-thiomorpholinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(4-pyridinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-{5-[3-(3-pyridinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[methyl(1-methyl-4-piperidinyl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{5-[3-(4-piperidinylamino)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[5-(3-{[(1-methyl-4-piperidinyl)methyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(methyl{2-[methyl(methylsulfonyl)amino]ethyl}amino)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[5-(3-{methyl[2-(methylamino)ethyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(methyl{2-[(methylsulfonyl)amino]ethyl}amino)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[(2-aminoethyl)(methyl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-{5-[3-({2-[(methylsulfonyl)amino]ethyl}amino)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-[5-(3-{[1-(methylsulfonyl)-4-piperidinyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide;-   N-{5-[3-(4-pyridazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide;-   N-(5-{3-[(1-methyl-4-piperidinyl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N,N-dimethyl-4-[(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)amino]-1-piperidinesulfonamide;-   N-(5-{3-[(1-{[4-(methyloxy)phenyl]sulfonyl}-4-piperidinyl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide;-   N-[3-(methyloxy)phenyl]-7-(3-pyridinyl)-2-quinoxalinamine;-   N-[2-(methyloxy)-5-(3-{[3-(methyloxy)phenyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide    and-   N-[2-chloro-5-(3-{[3-(methyloxy)phenyl]amino}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide.

This invention also relates to a method of treating cancer, whichcomprises co-administering to a subject in need thereof an effectiveamount of a compound of Formula (I), and/or a pharmaceuticallyacceptable salt thereof; and at least one anti-neoplastic agent such asone selected from the group consisting of: anti-microtubule agents,platinum coordination complexes, alkylating agents, antibiotic agents,topoisomerase II inhibitors, antimetabolites, topoisomerase Iinhibitors, hormones and hormonal analogues, signal transduction pathwayinhibitors, non-receptor tyrosine kinase angiogenesis inhibitors,immunotherapeutic agents, proapoptotic agents, and cell cycle signalinginhibitors.

This invention also relates to a method of treating cancer, whichcomprises co-administering to a subject in need thereof an effectiveamount of a compound of Formula (I), and/or a pharmaceuticallyacceptable salt thereof; and at least one signal transduction pathwayinhibitor such as one selected from the group consisting of: receptortyrosine kinase inhibitor, non-receptor tyrosine kinase inhibitor,SH2/SH3 domain blocker, serine/threonine kinase inhibitor, phosphotidylinositol-3 kinase inhibitor, myo-inositol signaling inhibitor, and Rasoncogene inhibitor.

As used herein, the term “effective amount” means that amount of a drugor pharmaceutical agent that will elicit the biological or medicalresponse of a tissue, system, animal or human that is being sought, forinstance, by a researcher or clinician. Furthermore, the term“therapeutically effective amount” means any amount which, as comparedto a corresponding subject who has not received such amount, results inimproved treatment, healing, prevention, or amelioration of a disease,disorder, or side effect, or a decrease in the rate of advancement of adisease or disorder. The term also includes within its scope amountseffective to enhance normal physiological function.

Compounds of Formula (I) are included in the pharmaceutical compositionsof the invention.

DEFINITIONS

By the term “substituted amino” as used herein, is meant —NR30R40wherein each R30 and R40 is independently selected from a groupincluding hydrogen, C1-6alkyl, acyl, C3-C7cycloalkyl, wherein at leastone of R30 and R40 is not hydrogen.

By the term “acyl” as used herein, unless otherwise defined, is meant—C(O)(alkyl), —C(O)(cycloalkyl), —C(O)(aryl) or —C(O)(heteroaryl),wherein heteroaryl and aryl are optionally substituted.

By the term “aryl” as used herein, unless otherwise defined, is meantaromatic, hydrocarbon, ring system. The ring system may be monocyclic orfused polycyclic (e.g. bicyclic, tricyclic, etc.). In variousembodiments, the monocyclic aryl ring is C5-C10, or C5-C7, or C5-C6,where these carbon numbers refer to the number of carbon atoms that formthe ring system. A C6 ring system, i.e. a phenyl ring is a suitable arylgroup. In various embodiments, the polycyclic ring is a bicyclic arylgroup, where suitable bicyclic aryl groups are C8-C12, or C9-C10. Anaphthyl ring, which has 10 carbon atoms, is a suitable polycyclic arylgroup.

By the term “heteroaryl” as used herein, unless otherwise defined, ismeant an aromatic ring system containing carbon(s) and at least oneheteroatom. Heteroaryl may be monocyclic or polycyclic. A monocyclicheteroaryl group may have 1 to 4 heteroatoms in the ring, while apolycyclic heteroaryl may contain 1 to 10 hetero atoms. A polycyclicheteroaryl ring may contain fused, spiro or bridged ring junctions, forexample, bicyclic heteroaryl is a polycyclic heteroaryl. Bicyclicheteroaryl rings may contain from 8 to 12 member atoms. Monocyclicheteroaryl rings may contain from 5 to 8 member atoms (carbons andheteroatoms). Exemplary heteroaryl groups include but are not limitedto: benzofuran, benzothiophene, furan, imidazole, indole, isothiazole,oxazole, pyrazine, pyrazole, pyridazine, pyridine, pyrimidine, pyrrole,quinoline, quinazoline, quinoxaline, thiazole, and thiophene.

By the term “monocyclic heteroaryl” as used herein, unless otherwisedefined, is meant a monocyclic heteroaryl ring containing 1-5 carbonatoms and 1-4 hetero atoms.

By the term “alkylcarboxy” as used herein, unless otherwise defined, ismeant —(CH₂)_(n)COOR₈₀, wherein R80 is hydrogen or C1-C6alkyl, n is 0-6.

By the term “alkoxy” as used herein is meant —O(alkyl) including —OCH₃,—OCH₂CH₃ and —OC(CH₃)₃ where alkyl is as described herein.

By the term “alkylthio” as used herein is meant —S(alkyl) including—SCH₃, —SCH₂CH₃ where alkyl is as described herein.

The term “cycloalkyl” as used herein unless otherwise defined, is meanta nonaromatic, unsaturated or saturated, cyclic or polycyclic C3-C12.

Examples of cycloalkyl and substituted cycloalkyl substituents as usedherein include: cyclohexyl, aminocyclohexyl, cyclobutyl,aminocyclobutyl, 4-hydroxy-cyclohexyl, 2-ethylcyclohexyl,propyl4-methoxycyclohexyl, 4-methoxycyclohexyl, 4-carboxycyclohexyl,cyclopropyl, aminocyclopentyl, and cyclopentyl.

By the term “heterocycloalkyl” as used herein is meant a non-aromatic,unsaturated or saturated, monocyclic or polycyclic, heterocyclic ringcontaining at least one carbon and at least one heteroatom. Exemplarymonocyclic heterocyclic rings include: piperidine, piperazine,pyrrolidine, and morpholine. Exemplary polycyclic heterocyclic ringsinclude quinuclidine.

By the term “substituted” as used herein, unless otherwise defined, ismeant that the subject chemical moiety has one to five substituents,suitably from one to three, selected from the group consisting of:hydrogen, halogen, C1-C6alkyl, amino, urea, trifluoromethyl,—(CH₂)_(n)COOH, C3-C7cycloalkyl, substituted amino, aryl, heteroaryl,arylalkyl, arylcycloalkyl, heteroarylalkyl, heterocycloalkyl, cyano,hydroxyl, alkoxy, alkylthio, aryloxy, acyloxy, acyl, acylamino,aminoacyl, arylamino, nitro, oxo, —CO₂R₅₀, —SO₂R₇₀, —NR₅₀SO₂R₇₀,NR₅₀C(O)R₇₅ and —CONR₅₅R₆₀, wherein R50 and R55 are each independentlyselected from: hydrogen, alkyl, and C3-C7cycloalkyl; R55 and R60 canoptionally form a heterocycloalkyl ring; n is 0 to 6; R75 is selectedfrom the group consisting of: C1-C6alkyl, C3-7cylcoalkyl, substitutedC3-7cycloalkyl, aryl, substituted aryl, heteroaryl, substitutedheteroaryl, amino, substituted amino, arylamino, C1-C6heterocycloalkyl,alkoxy, aryloxy and substituted C1-C6heterocycloalkyl; each R60 and R70is independently selected from the group consisting of: C1-C6alkyl,C3-C7cycloalkyl, substituted C1-C6heterocycloalkyl,C1-C6heterocycloalkyl, halogen, amino, substituted amino, arylamino,trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, —(CH₂)_(n)COOH, aryloptionally fused with a five-membered ring or substituted with one tofive groups selected from the group consisting of: C1-C6alkyl,C3-C7cycloalkyl, halogen, amino, substituted amino, trifluoromethyl,cyano, hydroxyl, alkoxy, oxo, or —(CH₂)_(n)COOH, or heteroaryloptionally fused with a five-membered ring or substituted with one tofive groups selected from the group consisting of: C1-C6alkyl,C3-C7cycloalkyl, halogen, amino, trifluoromethyl, cyano, hydroxyl,alkoxy, oxo, or —(CH₂)_(n)COOH.

By the term “substituted”, when referred in the definition of R60, R70,R75, “arylamino”, and “aryloxy”, is meant that the subject chemicalmoiety has one to five substituents, suitably from one to threesubstituents selected from the group consisting of: hydrogen,C1-C6alkyl, halogen, trifluoromethyl, —(CH₂)_(n)COOH, amino, substitutedamino, cyano, hydroxyl, alkoxy, alkylthio, aryloxy, acyloxy, acyl,acylamino, and nitro, n is 0-6.

By the term “acyloxy” as used herein is meant —OC(O)alkyl where alkyl isas described herein. Examples of acyloxy substituents as used hereininclude: —OC(O)CH₃, —OC(O)CH(CH₃)₂ and —OC(O)(CH₂)₃CH₃.

By the term “acylamino” as used herein is meant —N(H)C(O)alkyl,—N(H)C(O)(cycloalkyl) where alkyl is as described herein. Examples ofN-acylamino substituents as used herein include: —N(H)C(O)CH₃,—N(H)C(O)CH(CH₃)₂ and —N(H)C(O)(CH₂)₃CH₃.

By the term “aminoacyl” as used herein is meant —C(O)N(alkyl)_(n),—C(O)N(cycloalkyl)_(n) where alkyl is as described herein, n is 1-2.

By the term “aryloxy” as used herein is meant —O(aryl), —O(substitutedaryl), —O(heteroaryl) or —O(substituted heteroaryl).

By the term “arylamino” as used herein is meant —NR₈₀(aryl),—NR₈₀(substituted aryl), —NR₈₀(heteroaryl) or —NR₈₀(substitutedheteroaryl), wherein R₈₀ is H, C1-6alkyl or C3-C7cycloalkyl.

By the term “heteroatom” as used herein is meant oxygen, nitrogen orsulfur.

By the term “halogen” as used herein is meant a substituent selectedfrom bromide, iodide, chloride and fluoride.

By the term “alkyl” and derivatives thereof and in all carbon chains asused herein, including alkyl chains defined by the term “—(CH₂)_(n)”,“—(CH₂)_(m)” and the like, is meant a linear or branched, saturated orunsaturated hydrocarbon chain, and unless otherwise defined, the carbonchain will contain from 1 to 12 carbon atoms.

By the term “substituted alkyl” as used herein is meant an alkyl groupsubstituted with one to six substituents selected from the groupconsisting of: halogen, trifluoromethyl, alkylcarboxy, amino,substituted amino, cyano, hydroxyl, alkoxy, alkylthio, aryloxy, acyloxy,acyl, acylamino, carbamate, urea, sulfonamate, C3-7cycloheteroalkyl,C3-7cycloalkyl and nitro.

Examples of alkyl and substituted alkyl substituents as used hereininclude: —CH₃, —CH₂—CH₃, —CH₂—CH₂—CH₃, —CH(CH₃)₂, —CH₂—CH₂—C(CH₃)₃,—CH₂—CF₃, —C≡C—C(CH₃)₃, —C≡C—CH₂—OH, cyclopropylmethyl,—CH₂—C(CH₃)₂—CH₂—NH₂, —C≡C—C₆H₅, —C≡C—C(CH₃)₂—OH,—CH₂—CH(OH)—CH(OH)—CH(OH)—CH(OH)—CH₂—OH, piperidinylmethyl,methoxyphenylethyl, —C(CH₃)₃, —(CH₂)₃—CH₃, —CH₂—CH(CH₃)₂,—CH(CH₃)—CH₂—CH₃, —CH═CH₂, and —C≡C—CH₃.

By the term “treating” and derivatives thereof as used herein, is meantprophylatic and therapeutic therapy.

By the term “co-administering” and derivatives thereof as used herein ismeant either simultaneous administration or any manner of separatesequential administration of a PI3 kinase inhibiting compound, asdescribed herein, and a further active ingredient or ingredients, knownto be useful in the treatment of cancer, including chemotherapy andradiation treatment. The term further active ingredient or ingredients,as used herein, includes any compound or therapeutic agent known to orthat demonstrates advantageous properties when administered to a patientin need of treatment for cancer. Suitably, if the administration is notsimultaneous, the compounds are administered in a close time proximityto each other. Furthermore, it does not matter if the compounds areadministered in the same dosage form, e.g. one compound may beadministered topically and another compound may be administered orally.

The term “compound” as used herein includes all isomers of the compound.Examples of such isomers include: enantiomers, tautomers, rotamers.

In formula (II) to (VIII), when a “dot” bond is drawn between two atoms,it is meant that such bond can be either single or double bond. A ringsystem containing such bonds can be aromatic or non-aromatic.

Certain compounds described herein may contain one or more chiral atoms,or may otherwise be capable of existing as two enantiomers, or two ormore diastereoisomers. Accordingly, the compounds of this inventioninclude mixtures of enantiomers/diastereoisomers as well as purifiedenantiomers/diastereoisomers or enantiomerically/diastereoisomericallyenriched mixtures. Also included within the scope of the invention arethe individual isomers of the compounds represented by formula I or IIabove as well as any wholly or partially equilibrated mixtures thereof.The present invention also covers the individual isomers of thecompounds represented by the formulas above as mixtures with isomersthereof in which one or more chiral centers are inverted. Further, anexample of a possible tautomer is an oxo substituent in place of ahydroxy substituent. Also, as stated above, it is understood that alltautomers and mixtures of tautomers are included within the scope of thecompounds of Formula I or II.

Compounds of Formula (I) are included in the pharmaceutical compositionsof the invention. Where a —COOH or —OH group is present,pharmaceutically acceptable esters can be employed, for example methyl,ethyl, pivaloyloxymethyl, and the like for —COOH, and acetate maleateand the like for —OH, and those esters known in the art for modifyingsolubility or hydrolysis characteristics, for use as sustained releaseor prod rug formulations.

It has now been found that compounds of the present invention areinhibitors of the Phosphatoinositides 3-kinases (PI3Ks). When thephosphatoinositides 3-kinase (PI3K) enzyme is inhibited by a compound ofthe present invention, PI3K is unable to exert its enzymatic, biologicaland/or pharmacological effects. The compounds of the present inventionare therefore useful in the treatment of autoimmune disorders,inflammatory diseases, cardiovascular diseases, neurodegenerativediseases, allergy, asthma, pancreatitis, multiorgan failure, kidneydiseases, platelet aggregation, cancer, sperm motility, transplantationrejection, graft rejection and lung injuries.

The compounds of Formula (I) are useful as medicaments in particular forthe treatment of autoimmune disorders, inflammatory diseases,cardiovascular diseases, neurodegenerative diseases, allergy, asthma,pancreatitis, multiorgan failure, kidney diseases, platelet aggregation,cancer, sperm motility, transplantation rejection, graft rejection andlung injuries. According to one embodiment of the present invention, thecompounds of Formula (I) are inhibitors of one or morephosphatoinositides 3-kinases (PI3Ks), suitably, Phosphatoinositides3-kinase γ (PI3Kγ), Phosphatoinositides 3-kinase γ (PI3Kα),Phosphatoinositides 3-kinase γ (PI3Kβ), and/or Phosphatoinositides3-kinase γ (PI3Kδ).

Compounds according to Formula (I) are suitable for the modulation,notably the inhibition of the activity of phosphatoinositides 3-kinases(PI3K), suitably phosphatoinositides 3-kinase (PI3Kα). Therefore thecompounds of the present invention are also useful for the treatment ofdisorders which are mediated by PI3Ks. Said treatment involves themodulation—notably the inhibition or the down regulation—of thephosphatoinositides 3-kinases.

Suitably, the compounds of the present invention are used for thepreparation of a medicament for the treatment of a disorder selectedfrom multiple sclerosis, psoriasis, rheumatoid arthritis, systemic lupuserythematosis, inflammatory bowel disease, lung inflammation, thrombosisor brain infection/inflammation, such as meningitis or encephalitis,Alzheimer's disease, Huntington's disease, CNS trauma, stroke orischemic conditions, cardiovascular diseases such as athero-sclerosis,heart hypertrophy, cardiac myocyte dysfunction, elevated blood pressureor vasoconstriction.

Suitably, the compounds of Formula (I) are useful for the treatment ofautoimmune diseases or inflammatory diseases such as multiple sclerosis,psoriasis, rheumatoid arthritis, systemic lupus erythematosis,inflammatory bowel disease, lung inflammation, thrombosis or braininfection/inflammation such as meningitis or encephalitis.

Suitably, the compounds of Formula (I) are useful for the treatment ofneurodegenerative diseases including multiple sclerosis, Alzheimer'sdisease, Huntington's disease, CNS trauma, stroke or ischemicconditions.

Suitably, the compounds of Formula (I) are useful for the treatment ofcardiovascular diseases such as atherosclerosis, heart hypertrophy,cardiac myocyte dysfunction, elevated blood pressure orvasoconstriction.

Suitably, the compounds of Formula (I) are useful for the treatment ofchronic obstructive pulmonary disease, anaphylactic shock fibrosis,psoriasis, allergic diseases, asthma, stroke, ischemic conditions,ischemia-reperfusion, platelets aggregation/activation, skeletal muscleatrophy/hypertrophy, leukocyte recruitment in cancer tissue,angiogenesis, invasion metastasis, in particular melanoma, Karposi'ssarcoma, acute and chronic bacterial and viral infections, sepsis,transplantation rejection, graft rejection, glomerulo sclerosis,glomerulo nephritis, progressive renal fibrosis, endothelial andepithelial injuries in the lung, and lung airway inflammation.

Because the pharmaceutically active compounds of the present inventionare active as PI3 kinase inhibitors, particularly the compounds thatinhibit PI3Kα, either selectively or in conjunction with one or more ofPI3δ, PI3Kβ, and/or PI3Kγ, they exhibit therapeutic utility in treatingcancer.

Suitably, the invention relates to a method of treating cancer in amammal, including a human, wherein the cancer is selected from: brain(gliomas), glioblastomas, leukemias, Bannayan-Zonana syndrome, Cowdendisease, Lhermitte-Duclos disease, breast, inflammatory breast cancer,Wilm's tumor, Ewing's sarcoma, Rhabdomyosarcoma, ependymoma,medulloblastoma, colon, head and neck, kidney, lung, liver, melanoma,ovarian, pancreatic, prostate, sarcoma, osteosarcoma, giant cell tumorof bone and thyroid.

Suitably, the invention relates to a method of treating cancer in amammal, including a human, wherein the cancer is selected from:Lymphoblastic T cell leukemia, Chronic myelogenous leukemia, Chroniclymphocytic leukemia, Hairy-cell leukemia, acute lymphoblastic leukemia,acute myelogenous leukemia, Chronic neutrophilic leukemia, Acutelymphoblastic T cell leukemia, Plasmacytoma, Immunoblastic large cellleukemia, Mantle cell leukemia, Multiple myeloma Megakaryoblasticleukemia, multiple myeloma, Acute megakaryocytic leukemia, promyelocyticleukemia and Erythroleukemia.

Suitably, the invention relates to a method of treating cancer in amammal, including a human, wherein the cancer is selected from:malignant lymphoma, hodgkins lymphoma, non-hodgkins lymphoma,lymphoblastic T cell lymphoma, Burkitt's lymphoma and follicularlymphoma.

Suitably, the invention relates to a method of treating cancer in amammal, including a human, wherein the cancer is selected from:neuroblastoma, bladder cancer, urothelial cancer, lung cancer, vulvalcancer, cervical cancer, endometrial cancer, renal cancer, mesothelioma,esophageal cancer, salivary gland cancer, hepatocellular cancer, gastriccancer, nasopharangeal cancer, buccal cancer, cancer of the mouth, GIST(gastrointestinal stromal tumor) and testicular cancer.

When a compound of Formula (I) is administered for the treatment ofcancer, the term “co-administering” and derivatives thereof as usedherein is meant either simultaneous administration or any manner ofseparate sequential administration of a PI3 kinase inhibiting compound,as described herein, and a further active ingredient or ingredients,known to be useful in the treatment of cancer, including chemotherapyand radiation treatment. The term further active ingredient oringredients, as used herein, includes any compound or therapeutic agentknown to or that demonstrates advantageous properties when administeredto a patient in need of treatment for cancer. Preferably, if theadministration is not simultaneous, the compounds are administered in aclose time proximity to each other. Furthermore, it does not matter ifthe compounds are administered in the same dosage form, e.g. onecompound may be administered topically and another compound may beadministered orally.

Typically, any anti-neoplastic agent that has activity versus asusceptible tumor being treated may be co-administered in the treatmentof cancer in the present invention. Examples of such agents can be foundin Cancer Principles and Practice f Oncology by V. T. Devita and S.Hellman (editors), 6^(th) edition (Feb. 15, 2001), Lippincott Williams &Wilkins Publishers. A person of ordinary skill in the art would be ableto discern which combinations of agents would be useful based on theparticular characteristics of the drugs and the cancer involved. Typicalanti-neoplastic agents useful in the present invention include, but arenot limited to, anti-microtubule agents such as diterpenoids and vincaalkaloids; platinum coordination complexes; alkylating agents such asnitrogen mustards, oxazaphosphorines, alkylsulfonates, nitrosoureas, andtriazenes; antibiotic agents such as anthracyclines, actinomycins andbleomycins; topoisomerase II inhibitors such as epipodophyllotoxins;antimetabolites such as purine and pyrimidine analogues and anti-folatecompounds; topoisomerase I inhibitors such as camptothecins; hormonesand hormonal analogues; signal transduction pathway inhibitors;non-receptor tyrosine kinase angiogenesis inhibitors; immunotherapeuticagents; proapoptotic agents; and cell cycle signaling inhibitors.

Examples of a further active ingredient or ingredients for use incombination or co-administered with the present PI3 kinase inhibitingcompounds are chemotherapeutic agents.

Anti-microtubule or anti-mitotic agents are phase specific agents activeagainst the microtubules of tumor cells during M or the mitosis phase ofthe cell cycle. Examples of anti-microtubule agents include, but are notlimited to, diterpenoids and vinca alkaloids.

Diterpenoids, which are derived from natural sources, are phase specificanti-cancer agents that operate at the G₂/M phases of the cell cycle. Itis believed that the diterpenoids stabilize the β-tubulin subunit of themicrotubules, by binding with this protein. Disassembly of the proteinappears then to be inhibited with mitosis being arrested and cell deathfollowing. Examples of diterpenoids include, but are not limited to,paclitaxel and its analog docetaxel.

Paclitaxel, 5β,20-epoxy-1,2α,4,7β,10β,13α-hexa-hydroxytax-11-en-9-one4,10-diacetate 2-benzoate 13-ester with(2R,3S)—N-benzoyl-3-phenylisoserine; is a natural diterpene productisolated from the Pacific yew tree Taxus brevifolia and is commerciallyavailable as an injectable solution TAXOL®. It is a member of the taxanefamily of terpenes. It was first isolated in 1971 by Wani et al. J. Am.Chem, Soc., 93:2325. 1971), who characterized its structure by chemicaland X-ray crystallographic methods. One mechanism for its activityrelates to paclitaxel's capacity to bind tubulin, thereby inhibitingcancer cell growth. Schiff et al., Proc. Natl, Acad, Sci. USA,77:1561-1565 (1980); Schiff et al., Nature, 277:665-667 (1979); Kumar,J. Biol, Chem, 256: 10435-10441 (1981). For a review of synthesis andanticancer activity of some paclitaxel derivatives see: D. G. I.Kingston et al., Studies in Organic Chemistry vol. 26, entitled “Newtrends in Natural Products Chemistry 1986”, Attaur-Rahman, P. W. LeQuesne, Eds. (Elsevier, Amsterdam, 1986) pp 219-235.

Paclitaxel has been approved for clinical use in the treatment ofrefractory ovarian cancer in the United States (Markman et al., YaleJournal of Biology and Medicine, 64:583, 1991; McGuire et al., Ann.Intern, Med., 111:273, 1989) and for the treatment of breast cancer(Holmes et al., J. Nat. Cancer Inst., 83:1797, 1991.) It is a potentialcandidate for treatment of neoplasms in the skin (Einzig et. al., Proc.Am. Soc. Clin. Oncol., 20:46) and head and neck carcinomas (Forastireet. al., Sem. Oncol., 20:56, 1990). The compound also shows potentialfor the treatment of polycystic kidney disease (Woo et. al., Nature,368:750. 1994), lung cancer and malaria. Treatment of patients withpaclitaxel results in bone marrow suppression (multiple cell lineages,Ignoff, R. J. et. al, Cancer Chemotherapy Pocket Guide, 1998) related tothe duration of dosing above a threshold concentration (50 nM) (Kearns,C. M. et. al., Seminars in Oncology, 3(6) p. 16-23, 1995).

Docetaxel, (2R,3S)—N-carboxy-3-phenylisoserine, N-tert-butyl ester,13-ester with 5β-20-epoxy-1,2α,4,7β,10β,13α-hexahydroxytax-11-en-9-one4-acetate 2-benzoate, trihydrate; is commercially available as aninjectable solution as TAXOTERE®. Docetaxel is indicated for thetreatment of breast cancer. Docetaxel is a semisynthetic derivative ofpaclitaxel q.v., prepared using a natural precursor,10-deacetyl-baccatin III, extracted from the needle of the European Yewtree. The dose limiting toxicity of docetaxel is neutropenia.

Vinca alkaloids are phase specific anti-neoplastic agents derived fromthe periwinkle plant. Vinca alkaloids act at the M phase (mitosis) ofthe cell cycle by binding specifically to tubulin. Consequently, thebound tubulin molecule is unable to polymerize into microtubules.Mitosis is believed to be arrested in metaphase with cell deathfollowing. Examples of vinca alkaloids include, but are not limited to,vinblastine, vincristine, and vinorelbine.

Vinblastine, vincaleukoblastine sulfate, is commercially available asVELBAN® as an injectable solution. Although, it has possible indicationas a second line therapy of various solid tumors, it is primarilyindicated in the treatment of testicular cancer and various lymphomasincluding Hodgkin's Disease; and lymphocytic and histiocytic lymphomas.Myelosuppression is the dose limiting side effect of vinblastine.

Vincristine, vincaleukoblastine, 22-oxo-, sulfate, is commerciallyavailable as ONCOVIN® as an injectable solution. Vincristine isindicated for the treatment of acute leukemias and has also found use intreatment regimens for Hodgkin's and non-Hodgkin's malignant lymphomas.Alopecia and neurologic effects are the most common side effect ofvincristine and to a lesser extent myelosupression and gastrointestinalmucositis effects occur.

Vinorelbine,3′,4′-didehydro-4′-deoxy-C′-norvincaleukoblastine[R—(R*,R*)-2,3-dihydroxybutanedioate(1:2)(salt)], commercially available as an injectable solution ofvinorelbine tartrate (NAVELBINE®), is a semisynthetic vinca alkaloid.Vinorelbine is indicated as a single agent or in combination with otherchemotherapeutic agents, such as cisplatin, in the treatment of varioussolid tumors, particularly non-small cell lung, advanced breast, andhormone refractory prostate cancers. Myelosuppression is the most commondose limiting side effect of vinorelbine.

Platinum coordination complexes are non-phase specific anti-canceragents, which are interactive with DNA. The platinum complexes entertumor cells, undergo, aquation and form intra- and interstrandcrosslinks with DNA causing adverse biological effects to the tumor.Examples of platinum coordination complexes include, but are not limitedto, cisplatin and carboplatin.

Cisplatin, cis-diaminedichloroplatinum, is commercially available asPLATINOL® as an injectable solution. Cisplatin is primarily indicated inthe treatment of metastatic testicular and ovarian cancer and advancedbladder cancer. The primary dose limiting side effects of cisplatin arenephrotoxicity, which may be controlled by hydration and diuresis, andototoxicity.

Carboplatin, platinum, diamine[1,1-cyclobutane-dicarboxylate(2-)-O,O′],is commercially available as PARAPLATIN® as an injectable solution.Carboplatin is primarily indicated in the first and second linetreatment of advanced ovarian carcinoma. Bone marrow suppression is thedose limiting toxicity of carboplatin.

Alkylating agents are non-phase anti-cancer specific agents and strongelectrophiles. Typically, alkylating agents form covalent linkages, byalkylation, to DNA through nucleophilic moieties of the DNA moleculesuch as phosphate, amino, sulfhydryl, hydroxyl, carboxyl, and imidazolegroups. Such alkylation disrupts nucleic acid function leading to celldeath. Examples of alkylating agents include, but are not limited to,nitrogen mustards such as cyclophosphamide, melphalan, and chlorambucil;alkyl sulfonates such as busulfan; nitrosoureas such as carmustine; andtriazenes such as dacarbazine.

Cyclophosphamide,2-[bis(2-chloroethyl)amino]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxidemonohydrate, is commercially available as an injectable solution ortablets as CYTOXAN®. Cyclophosphamide is indicated as a single agent orin combination with other chemotherapeutic agents, in the treatment ofmalignant lymphomas, multiple myeloma, and leukemias. Alopecia, nausea,vomiting and leukopenia are the most common dose limiting side effectsof cyclophosphamide.

Melphalan, 4-[bis(2-chloroethyl)amino]-L-phenylalanine, is commerciallyavailable as an injectable solution or tablets as ALKERAN®. Melphalan isindicated for the palliative treatment of multiple myeloma andnon-respectable epithelial carcinoma of the ovary. Bone marrowsuppression is the most common dose limiting side effect of melphalan.

Chlorambucil, 4-[bis(2-chloroethyl)amino]benzenebutanoic acid, iscommercially available as LEUKERAN® tablets. Chlorambucil is indicatedfor the palliative treatment of chronic lymphatic leukemia, andmalignant lymphomas such as lymphosarcoma, giant follicular lymphoma,and Hodgkin's disease. Bone marrow suppression is the most common doselimiting side effect of chlorambucil.

Busulfan, 1,4-butanediol dimethanesulfonate, is commercially availableas MYLERAN® TABLETS. Busulfan is indicated for the palliative treatmentof chronic myelogenous leukemia. Bone marrow suppression is the mostcommon dose limiting side effects of busulfan.

Carmustine, 1,3-[bis(2-chloroethyl)-1-nitrosourea, is commerciallyavailable as single vials of lyophilized material as BiCNU®. Carmustineis indicated for the palliative treatment as a single agent or incombination with other agents for brain tumors, multiple myeloma,Hodgkin's disease, and non-Hodgkin's lymphomas. Delayed myelosuppressionis the most common dose limiting side effects of carmustine.

Dacarbazine, 5-(3,3-dimethyl-1-triazeno)-imidazole-4-carboxamide, iscommercially available as single vials of material as DTIC-Dome®.Dacarbazine is indicated for the treatment of metastatic malignantmelanoma and in combination with other agents for the second linetreatment of Hodgkin's Disease. Nausea, vomiting, and anorexia are themost common dose limiting side effects of dacarbazine.

Antibiotic anti-neoplastics are non-phase specific agents, which bind orintercalate with DNA. Typically, such action results in stable DNAcomplexes or strand breakage, which disrupts ordinary function of thenucleic acids leading to cell death. Examples of antibioticanti-neoplastic agents include, but are not limited to, actinomycinssuch as dactinomycin, anthrocyclins such as daunorubicin anddoxorubicin; and bleomycins.

Dactinomycin, also know as Actinomycin D, is commercially available ininjectable form as COSMEGEN®. Dactinomycin is indicated for thetreatment of Wilm's tumor and rhabdomyosarcoma. Nausea, vomiting, andanorexia are the most common dose limiting side effects of dactinomycin.

Daunorubicin,(8S-cis-)-8-acetyl-10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12naphthacenedione hydrochloride, is commercially available as a liposomalinjectable form as DAUNOXOME® or as an injectable as CERUBIDINE®.Daunorubicin is indicated for remission induction in the treatment ofacute nonlymphocytic leukemia and advanced HIV associated Kaposi'ssarcoma. Myelosuppression is the most common dose limiting side effectof daunorubicin.

Doxorubicin,(8S,10S)-10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-glycoloyl,7,8,9,10-tetrahydro-6,8,11-tri hydroxy-1-methoxy-5,12 naphthacenedionehydrochloride, is commercially available as an injectable form as RUBEX®or ADRIAMYCIN RDF®. Doxorubicin is primarily indicated for the treatmentof acute lymphoblastic leukemia and acute myeloblastic leukemia, but isalso a useful component in the treatment of some solid tumors andlymphomas. Myelosuppression is the most common dose limiting side effectof doxorubicin.

Bleomycin, a mixture of cytotoxic glycopeptide antibiotics isolated froma strain of Streptomyces verticillus, is commercially available asBLENOXANE®. Bleomycin is indicated as a palliative treatment, as asingle agent or in combination with other agents, of squamous cellcarcinoma, lymphomas, and testicular carcinomas. Pulmonary and cutaneoustoxicities are the most common dose limiting side effects of bleomycin.

Topoisomerase II inhibitors include, but are not limited to,epipodophyllotoxins.

Epipodophyllotoxins are phase specific anti-neoplastic agents derivedfrom the mandrake plant. Epipodophyllotoxins typically affect cells inthe S and G₂ phases of the cell cycle by forming a ternary complex withtopoisomerase II and DNA causing DNA strand breaks. The strand breaksaccumulate and cell death follows. Examples of epipodophyllotoxinsinclude, but are not limited to, etoposide and teniposide.

Etoposide, 4′-demethyl-epipodophyllotoxin9[4,6-0-(R)-ethylidene-8-D-glucopyranoside], is commercially availableas an injectable solution or capsules as VePESID® and is commonly knownas VP-16. Etoposide is indicated as a single agent or in combinationwith other chemotherapy agents in the treatment of testicular andnon-small cell lung cancers. Myelosuppression is the most common sideeffect of etoposide. The incidence of leucopenia tends to be more severethan thrombocytopenia.

Teniposide, 4′-demethyl-epipodophyllotoxin9[4,6-0-(R)-thenylidene-8-D-glucopyranoside], is commercially availableas an injectable solution as VUMON® and is commonly known as VM-26.Teniposide is indicated as a single agent or in combination with otherchemotherapy agents in the treatment of acute leukemia in children.Myelosuppression is the most common dose limiting side effect ofteniposide. Teniposide can induce both leucopenia and thrombocytopenia.

Antimetabolite neoplastic agents are phase specific anti-neoplasticagents that act at S phase (DNA synthesis) of the cell cycle byinhibiting DNA synthesis or by inhibiting purine or pyrimidine basesynthesis and thereby limiting DNA synthesis. Consequently, S phase doesnot proceed and cell death follows. Examples of antimetaboliteanti-neoplastic agents include, but are not limited to, fluorouracil,methotrexate, cytarabine, mercaptopurine, thioguanine, and gemcitabine.

5-fluorouracil, 5-fluoro-2,4-(1H,3H) pyrimidinedione, is commerciallyavailable as fluorouracil. Administration of 5-fluorouracil leads toinhibition of thymidylate synthesis and is also incorporated into bothRNA and DNA. The result typically is cell death. 5-fluorouracil isindicated as a single agent or in combination with other chemotherapyagents in the treatment of carcinomas of the breast, colon, rectum,stomach and pancreas. Myelosuppression and mucositis are dose limitingside effects of 5-fluorouracil. Other fluoropyrimidine analogs include5-fluoro deoxyuridine (floxuridine) and 5-fluorodeoxyuridinemonophosphate.

Cytarabine, 4-amino-1-β-D-arabinofuranosyl-2(1H)-pyrimidinone, iscommercially available as CYTOSAR-U® and is commonly known as Ara-C. Itis believed that cytarabine exhibits cell phase specificity at S-phaseby inhibiting DNA chain elongation by terminal incorporation ofcytarabine into the growing DNA chain. Cytarabine is indicated as asingle agent or in combination with other chemotherapy agents in thetreatment of acute leukemia. Other cytidine analogs include5-azacytidine and 2′,2′-difluorodeoxycytidine (gemcitabine). Cytarabineinduces leucopenia, thrombocytopenia, and mucositis.

Mercaptopurine, 1,7-dihydro-6H-purine-6-thione monohydrate, iscommercially available as PURINETHOL®. Mercaptopurine exhibits cellphase specificity at S-phase by inhibiting DNA synthesis by an as of yetunspecified mechanism. Mercaptopurine is indicated as a single agent orin combination with other chemotherapy agents in the treatment of acuteleukemia. Myelosuppression and gastrointestinal mucositis are expectedside effects of mercaptopurine at high doses. A useful mercaptopurineanalog is azathioprine.

Thioguanine, 2-amino-1,7-dihydro-6H-purine-6-thione, is commerciallyavailable as TABLOID®. Thioguanine exhibits cell phase specificity atS-phase by inhibiting DNA synthesis by an as of yet unspecifiedmechanism. Thioguanine is indicated as a single agent or in combinationwith other chemotherapy agents in the treatment of acute leukemia.Myelosuppression, including leucopenia, thrombocytopenia, and anemia, isthe most common dose limiting side effect of thioguanine administration.However, gastrointestinal side effects occur and can be dose limiting.Other purine analogs include pentostatin, erythrohydroxynonyladenine,fludarabine phosphate, and cladribine.

Gemcitabine, 2′-deoxy-2′,2′-difluorocytidine monohydrochloride(β-isomer), is commercially available as GEMZAR®. Gemcitabine exhibitscell phase specificity at S-phase and by blocking progression of cellsthrough the G1/S boundary. Gemcitabine is indicated in combination withcisplatin in the treatment of locally advanced non-small cell lungcancer and alone in the treatment of locally advanced pancreatic cancer.Myelosuppression, including leucopenia, thrombocytopenia, and anemia, isthe most common dose limiting side effect of gemcitabine administration.

Methotrexate,N-[4[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamicacid, is commercially available as methotrexate sodium. Methotrexateexhibits cell phase effects specifically at S-phase by inhibiting DNAsynthesis, repair and/or replication through the inhibition ofdyhydrofolic acid reductase which is required for synthesis of purinenucleotides and thymidylate. Methotrexate is indicated as a single agentor in combination with other chemotherapy agents in the treatment ofchoriocarcinoma, meningeal leukemia, non-Hodgkin's lymphoma, andcarcinomas of the breast, head, neck, ovary and bladder.Myelosuppression (leucopenia, thrombocytopenia, and anemia) andmucositis are expected side effect of methotrexate administration.

Camptothecins, including, camptothecin and camptothecin derivatives areavailable or under development as Topoisomerase I inhibitors.Camptothecins cytotoxic activity is believed to be related to itsTopoisomerase I inhibitory activity. Examples of camptothecins include,but are not limited to irinotecan, topotecan, and the various opticalforms of7-(4-methylpiperazino-methylene)-10,11-ethylenedioxy-20-camptothecindescribed below.

Irinotecan HCl, (4S)-4,11-diethyl-4-hydroxy-9-[(4-piperidinopiperidino)carbonyloxy]-1H-pyrano[3′,4′,6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dionehydrochloride, is commercially available as the injectable solutionCAMPTOSAR®.

Irinotecan is a derivative of camptothecin which binds, along with itsactive metabolite SN-38, to the topoisomerase I-DNA complex. It isbelieved that cytotoxicity occurs as a result of irreparable doublestrand breaks caused by interaction of the topoisomerase I:DNA:irintecanor SN-38 ternary complex with replication enzymes. Irinotecan isindicated for treatment of metastatic cancer of the colon or rectum. Thedose limiting side effects of irinotecan HCl are myelosuppression,including neutropenia, and GI effects, including diarrhea.

Topotecan HCl,(S)-10-[(dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-1H-pyrano[3′,4′,6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dionemonohydrochloride, is commercially available as the injectable solutionHYCAMTIN®. Topotecan is a derivative of camptothecin which binds to thetopoisomerase I-DNA complex and prevents religation of singles strandbreaks caused by Topoisomerase I in response to torsional strain of theDNA molecule. Topotecan is indicated for second line treatment ofmetastatic carcinoma of the ovary and small cell lung cancer. The doselimiting side effect of topotecan HCl is myelosuppression, primarilyneutropenia.

Also of interest, is the camptothecin derivative of formula A following,currently under development, including the racemic mixture (R,S) form aswell as the R and S enantiomers:

known by the chemical name“7-(4-methylpiperazino-methylene)-10,11-ethylenedioxy-20(R,S)-camptothecin(racemic mixture) or“7-(4-methylpiperazino-methylene)-10,11-ethylenedioxy-20(R)-camptothecin(R enantiomer) or“7-(4-methylpiperazino-methylene)-10,11-ethylenedioxy-20(S)-camptothecin(S enantiomer). Such compound as well as related compounds aredescribed, including methods of making, in U.S. Pat. Nos. 6,063,923;5,342,947; 5,559,235; 5,491,237 and pending U.S. patent application Ser.No. 08/977,217 filed Nov. 24, 1997.

Hormones and hormonal analogues are useful compounds for treatingcancers in which there is a relationship between the hormone(s) andgrowth and/or lack of growth of the cancer. Examples of hormones andhormonal analogues useful in cancer treatment include, but are notlimited to, adrenocorticosteroids such as prednisone and prednisolonewhich are useful in the treatment of malignant lymphoma and acuteleukemia in children; aminoglutethimide and other aromatase inhibitorssuch as anastrozole, letrazole, vorazole, and exemestane useful in thetreatment of adrenocortical carcinoma and hormone dependent breastcarcinoma containing estrogen receptors; progestins such as megestrolacetate useful in the treatment of hormone dependent breast cancer andendometrial carcinoma; estrogens, androgens, and anti-androgens such asflutamide, nilutamide, bicalutamide, cyproterone acetate and5α-reductases such as finasteride and dutasteride, useful in thetreatment of prostatic carcinoma and benign prostatic hypertrophy;anti-estrogens such as tamoxifen, toremifene, raloxifene, droloxifene,iodoxyfene, as well as selective estrogen receptor modulators (SERMS)such those described in U.S. Pat. Nos. 5,681,835, 5,877,219, and6,207,716, useful in the treatment of hormone dependent breast carcinomaand other susceptible cancers; and gonadotropin-releasing hormone (GnRH)and analogues thereof which stimulate the release of leutinizing hormone(LH) and/or follicle stimulating hormone (FSH) for the treatmentprostatic carcinoma, for instance, LHRH agonists and antagonists such asgoserelin acetate and luprolide.

Signal transduction pathway inhibitors are those inhibitors, which blockor inhibit a chemical process which evokes an intracellular change. Asused herein this change is cell proliferation or differentiation. Signaltransduction inhibitors useful in the present invention includeinhibitors of receptor tyrosine kinases, non-receptor tyrosine kinases,SH2/SH3domain blockers, serine/threonine kinases, phosphotidylinositol-3 kinases, myo-inositol signaling, and Ras oncogenes.

Several protein tyrosine kinases catalyse the phosphorylation ofspecific tyrosyl residues in various proteins involved in the regulationof cell growth. Such protein tyrosine kinases can be broadly classifiedas receptor or non-receptor kinases.

Receptor tyrosine kinases are transmembrane proteins having anextracellular ligand binding domain, a transmembrane domain, and atyrosine kinase domain. Receptor tyrosine kinases are involved in theregulation of cell growth and are generally termed growth factorreceptors. Inappropriate or uncontrolled activation of many of thesekinases, i.e. aberrant kinase growth factor receptor activity, forexample by over-expression or mutation, has been shown to result inuncontrolled cell growth. Accordingly, the aberrant activity of suchkinases has been linked to malignant tissue growth. Consequently,inhibitors of such kinases could provide cancer treatment methods.Growth factor receptors include, for example, epidermal growth factorreceptor (EGFr), platelet derived growth factor receptor (PDGFr), erbB2,erbB4, vascular endothelial growth factor receptor (VEGFr), tyrosinekinase with immunoglobulin-like and epidermal growth factor homologydomains (TIE-2), insulin growth factor-I (IGFI) receptor, macrophagecolony stimulating factor (cfms), BTK, ckit, cmet, fibroblast growthfactor (FGF) receptors, Trk receptors (TrkA, TrkB, and TrkC), ephrin(eph) receptors, and the RET protooncogene. Several inhibitors of growthreceptors are under development and include ligand antagonists,antibodies, tyrosine kinase inhibitors and anti-sense oligonucleotides.Growth factor receptors and agents that inhibit growth factor receptorfunction are described, for instance, in Kath, John C., Exp. Opin. Ther.Patents (2000) 10(6):803-818; Shawver et al DDT Vol 2, No. 2 Feb. 1997;and Lofts, F. J. et al, “Growth factor receptors as targets”, NewMolecular Targets for Cancer Chemotherapy, ed. Workman, Paul and Kerr,David, CRC press 1994, London.

Tyrosine kinases, which are not growth factor receptor kinases aretermed non-receptor tyrosine kinases. Non-receptor tyrosine kinasesuseful in the present invention, which are targets or potential targetsof anti-cancer drugs, include cSrc, Lck, Fyn, Yes, Jak, cAbl, FAK (Focaladhesion kinase), Brutons tyrosine kinase, and Bcr-Abl. Suchnon-receptor kinases and agents which inhibit non-receptor tyrosinekinase function are described in Sinh, S, and Corey, S. J., (1999)Journal of Hematotherapy and Stem Cell Research 8 (5): 465-80; andBolen, J. B., Brugge, J. S., (1997) Annual review of Immunology. 15:371-404.

SH2/SH3 domain blockers are agents that disrupt SH2 or SH3 domainbinding in a variety of enzymes or adaptor proteins including, PI3-K p85subunit, Src family kinases, adaptor molecules (Shc, Crk, Nck, Grb2) andRas-GAP. SH2/SH3 domains as targets for anti-cancer drugs are discussedin Smithgall, T. E. (1995), Journal of Pharmacological and ToxicologicalMethods. 34(3) 125-32.

Inhibitors of Serine/Threonine Kinases including MAP kinase cascadeblockers which include blockers of Raf kinases (rafk), Mitogen orExtracellular Regulated Kinase (MEKs), and Extracellular RegulatedKinases (ERKs); and Protein kinase C family member blockers includingblockers of PKCs (alpha, beta, gamma, epsilon, mu, lambda, iota, zeta).IkB kinase family (IKKa, IKKb), PKB family kinases, AKT kinase familymembers, and TGF beta receptor kinases. Such Serine/Threonine kinasesand inhibitors thereof are described in Yamamoto, T., Taya, S.,Kaibuchi, K., (1999), Journal of Biochemistry. 126 (5) 799-803; Brodt,P, Samani, A., and Navab, R. (2000), Biochemical Pharmacology, 60.1101-1107; Massague, J., Weis-Garcia, F. (1996) Cancer Surveys.27:41-64; Philip, P. A., and Harris, A. L. (1995), Cancer Treatment andResearch. 78: 3-27, Lackey, K. et al Bioorganic and Medicinal ChemistryLetters, (10), 2000, 223-226; U.S. Pat. No. 6,268,391; andMartinez-Iacaci, L., et al, Int. J. Cancer (2000), 88(1), 44-52.

Inhibitors of Phosphotidyl inositol-3 Kinase family members includingblockers of PI3-kinase, ATM, DNA-PK, and Ku are also useful in thepresent invention. Such kinases are discussed in Abraham, R. T. (1996),Current Opinion in Immunology. 8 (3) 412-8; Canman, C. E., Lim, D. S.(1998), Oncogene 17 (25) 3301-3308; Jackson, S. P. (1997), InternationalJournal of Biochemistry and Cell Biology. 29 (7):935-8; and Zhong, H. etal, Cancer res, (2000) 60(6), 1541-1545.

Also useful in the present invention are Myo-inositol signalinginhibitors such as phospholipase C blockers and Myoinositol analogues.Such signal inhibitors are described in Powis, G., and Kozikowski A.,(1994) New Molecular Targets for Cancer Chemotherapy ed., Paul Workmanand David Kerr, CRC press 1994, London.

Another group of signal transduction pathway inhibitors are inhibitorsof Ras Oncogene. Such inhibitors include inhibitors offarnesyltransferase, geranyl-geranyl transferase, and CAAX proteases aswell as anti-sense oligonucleotides, ribozymes and immunotherapy. Suchinhibitors have been shown to block ras activation in cells containingwild type mutant ras, thereby acting as antiproliferation agents. Rasoncogene inhibition is discussed in Scharovsky, O. G., Rozados, V. R.,Gervasoni, S. I. Matar, P. (2000), Journal of Biomedical Science. 7(4)292-8; Ashby, M. N. (1998), Current Opinion in Lipidology. 9 (2) 99-102;and BioChim. Biophys. Acta, (19899) 1423(3):19-30.

As mentioned above, antibody antagonists to receptor kinase ligandbinding may also serve as signal transduction inhibitors. This group ofsignal transduction pathway inhibitors includes the use of humanizedantibodies to the extracellular ligand binding domain of receptortyrosine kinases. For example Imclone C225 EGFR specific antibody (seeGreen, M. C. et al, Monoclonal Antibody Therapy for Solid Tumors, CancerTreat. Rev., (2000), 26(4), 269-286); Herceptin® erbB2 antibody (seeTyrosine Kinase Signalling in Breast cancer:erbB Family ReceptorTyrosine Kinases, Breast cancer Res., 2000, 2(3), 176-183); and 2CBVEGFR2 specific antibody (see Brekken, R. A. et al, Selective Inhibitionof VEGFR2 Activity by a monoclonal Anti-VEGF antibody blocks tumorgrowth in mice, Cancer Res. (2000) 60, 5117-5124).

Non-receptor kinase angiogenesis inhibitors may also find use in thepresent invention. Inhibitors of angiogenesis related VEGFR and TIE2 arediscussed above in regard to signal transduction inhibitors (bothreceptors are receptor tyrosine kinases). Angiogenesis in general islinked to erbB2/EGFR signaling since inhibitors of erbB2 and EGFR havebeen shown to inhibit angiogenesis, primarily VEGF expression. Thus, thecombination of an erbB2/EGFR inhibitor with an inhibitor of angiogenesismakes sense. Accordingly, non-receptor tyrosine kinase inhibitors may beused in combination with the EGFR/erbB2 inhibitors of the presentinvention. For example, anti-VEGF antibodies, which do not recognizeVEGFR (the receptor tyrosine kinase), but bind to the ligand; smallmolecule inhibitors of integrin (alpha_(v) beta₃) that will inhibitangiogenesis; endostatin and angiostatin (non-RTK) may also prove usefulin combination with the disclosed erb family inhibitors. (See Bruns C Jet al (2000), Cancer Res., 60: 2926-2935; Schreiber A B, Winkler M E,and Derynck R. (1986), Science, 232: 1250-1253; Yen L et al. (2000),Oncogene 19: 3460-3469).

Agents used in immunotherapeutic regimens may also be useful incombination with the compounds of formula (I). There are a number ofimmunologic strategies to generate an immune response against erbB2 orEGFR. These strategies are generally in the realm of tumor vaccinations.The efficacy of immunologic approaches may be greatly enhanced throughcombined inhibition of erbB2/EGFR signaling pathways using a smallmolecule inhibitor. Discussion of the immunologic/tumor vaccine approachagainst erbB2/EGFR are found in Reilly R T et al. (2000), Cancer Res.60: 3569-3576; and Chen Y, Hu D, Eling D J, Robbins J, and Kipps T J.(1998), Cancer Res. 58: 1965-1971.

Agents used in proapoptotic regimens (e.g., bcl-2 antisenseoligonucleotides) may also be used in the combination of the presentinvention. Members of the Bcl-2 family of proteins block apoptosis.Upregulation of bcl-2 has therefore been linked to chemoresistance.Studies have shown that the epidermal growth factor (EGF) stimulatesanti-apoptotic members of the bcl-2 family (i.e., mcl-1). Therefore,strategies designed to downregulate the expression of bcl-2 in tumorshave demonstrated clinical benefit and are now in Phase II/III trials,namely Genta's G3139 bcl-2 antisense oligonucleotide. Such proapoptoticstrategies using the antisense oligonucleotide strategy for bcl-2 arediscussed in Water J S et al. (2000), J. Clin. Oncol. 18: 1812-1823; andKitada S et al. (1994), Antisense Res. Dev. 4: 71-79.

Cell cycle signalling inhibitors inhibit molecules involved in thecontrol of the cell cycle. A family of protein kinases called cyclindependent kinases (CDKs) and their interaction with a family of proteinstermed cyclins controls progression through the eukaryotic cell cycle.The coordinate activation and inactivation of different cyclin/CDKcomplexes is necessary for normal progression through the cell cycle.Several inhibitors of cell cycle signalling are under development. Forinstance, examples of cyclin dependent kinases, including CDK2, CDK4,and CDK6 and inhibitors for the same are described in, for instance,Rosania et al, Exp. Opin. Ther. Patents (2000) 10(2):215-230.

In one embodiment, the cancer treatment method of the claimed inventionincludes the co-administration a compound of formula I and/or apharmaceutically acceptable salt, hydrate, solvate or pro-drug thereofand at least one anti-neoplastic agent, such as one selected from thegroup consisting of anti-microtubule agents, platinum coordinationcomplexes, alkylating agents, antibiotic agents, topoisomerase IIinhibitors, antimetabolites, topoisomerase I inhibitors, hormones andhormonal analogues, signal transduction pathway inhibitors, non-receptortyrosine kinase angiogenesis inhibitors, immunotherapeutic agents,proapoptotic agents, and cell cycle signaling inhibitors.

Because the pharmaceutically active compounds of the present inventionare active as PI3 kinase inhibitors, particularly the compounds thatmodulate/inhibit PI3Kα, either selectively or in conjunction with one ormore of PI3Kγ, PI3Kβ, and/or PI3δ, they exhibit therapeutic utility intreating a disease state selected from: autoimmune disorders,inflammatory diseases, cardiovascular diseases, neurodegenerativediseases, allergy, cancer, asthma, pancreatitis, multiorgan failure,kidney diseases, platelet aggregation, sperm motility, transplantationrejection, graft rejection and lung injuries.

When a compound of Formula (I) is administered for the treatment of adisease state selected from: autoimmune disorders, inflammatorydiseases, cardiovascular diseases, neurodegenerative diseases, cancer,allergy, asthma, pancreatitis, multiorgan failure, kidney diseases,platelet aggregation, sperm motility, transplantation rejection, graftrejection or lung injuries, the term “co-administering” and derivativesthereof as used herein is meant either simultaneous administration orany manner of separate sequential administration of a PI3 kinaseinhibiting compound, as described herein, and a further activeingredient or ingredients, known to be useful in the treatment ofautoimmune disorders, inflammatory diseases, cardiovascular diseases,cancer, neurodegenerative diseases, allergy, asthma, pancreatitis,multiorgan failure, kidney diseases, platelet aggregation, spermmotility, transplantation rejection, graft rejection and/or lunginjuries.

Biological Assays PI3K Alpha Leadseeker SPA Assay

Compounds of the present invention were tested according to thefollowing assays and found as inhibitors of PI3 kinases, particularlyPI3Kα. The exemplified compounds were tested and found active againstPI3Kα. The IC₅₀'s ranged from about 1 nM to 10 μM. The majority of thecompounds were under 500 nM; the most active compounds were under 10 nM.

The compound of Example 1 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 5 nM against PI3Kα.

The compound of Example 2 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 100 nM against PI3Kα.

The compound of Example 4 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 50 nM against PI3Kα.

The compound of Example 19 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 8 nM against PI3Kα.

The compound of Example 20 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 16 nM against PI3Kα.

The compound of Example 69 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 13 nM against PI3Kα.

The compound of Example 70 was tested generally according to the assaysdescribed herein and in at least one experimental run exhibited a IC50value: equal to 200 nM against PI3Kα.

Assay Principle

SPA imaging beads are microspheres containing scintillant which emitlight in the red region of the visible spectrum. As a result, thesebeads are ideally suited to use with a CCD imager such as the Viewlux.The Leadseeker beads used in this system are polystyrene beads that havebeen coupled with polyethyleneimine. When added to the assay mixture,the beads absorb both the substrate (PIP2) and product (PIP3). AdsorbedP³³-PIP3 will cause an increase in signal, measured as ADUs (analog todigital units). This protocol details the use of the PEI-PS Leadseekerbeads for assays using His-p110/p85 PI3K alpha.

Assay Protocol

Solid compounds are typically plated with 0.1 μl of 100% DMSO in allwells (except column 6 and 18) of a 384-well, flat bottom, low volumeplate (Greiner 784075). The compounds are serially diluted (3-fold in100% DMSO) across the plate from column 1 to column 12 and column 13 tocolumn 24 and leave column 6 and 18 containing only DMSO to yield 11concentrations for each test compound.

The assay buffer contains MOPS (pH 6.5), CHAPS, and DTT. PI3K alpha andPIP2 (L-alpha-D-myo-Phosphatidylinositol4,5-bisphosphate[PI(4,5)P2]3-O-phospho linked,D(+)-sn-1,2-di-O-octanoylglyceryl, CellSignals # 901) are mixed andincubated in the plate with compound for 30 min prior to starting thereaction with the addition of P³³-ATP and MgCl₂ (reagents added usingZoom). Enzyme-free wells (column 18) are typically done to determine thelow control. PEI-PS Leadseeker beads in PBS/EDTA/CHAPS are added (byMultidrop) to quench the reaction, and the plates are allowed toincubate for at least one hour (typically overnight) beforecentrifugation. The signal is determined using a Viewlux detector and isthen imported into curve fitting software (Activity Base) forconstruction of concentration response curves. The percent inhibition ofactivity is calculated relative to high controls (C1, 0.1 μl DMSO incolumn 6, rows A-P)) and low controls (C2, 5 μl of 40 uM PIP2 in bufferin column 18, rows A-P) using, 100*(1−(U1−C2)/(C1−C2)). Theconcentration of test compound yielding 50% inhibition is determinedusing the equation, y=((Vmax*x)/(K+x))+Y2, where “K” was equal to the1050. The IC50 values are converted to pIC50 values, i.e., −log IC50 inMolar concentration.

Cellular Assays:

Day 1

-   -   Plate cells before noon        -   10K cells/well in clear flat-bottomed 96-well plates (f.v.            105 ul)        -   Last four wells in last column receive media only        -   Place in 37 degC incubator overnight    -   Compound plate        -   Prepare in polypropylene round-bottomed 96-well plates; 8            compounds per        -   plate, 11-pt titrations of each (3× serial dilution), DMSO            in last column (0.15% f.c. on cells)        -   15 ul in first well, 10 ul DMSO in the rest; take 5 ul from            first well and mix in next, continue across plate (excluding            last column); seal with foil lid and place at 4 degC

Day 2

-   -   Take out Lysis buffer inhibitors (4 degC/−20 degC) and compound        plates (4 degC), thaw on bench top; make 1× Tris wash buffer        (WB) to fill reservoir on plate washer and top off bench supply        (use MiliQ), turn on centrifuge to allow it to cool    -   Block MSD plates        -   Make 20 ml 3% blocking solution/plate (600 mg blocker A in            20 ml WB), add 150 ul/well and incubate at RT for at least 1            hr    -   Add compound (while blocking)        -   Add 300 ul growth media (RPMI w/ Q, 10% FBS) per well            (682×dil of compound) to each compound plate        -   Add 5 ul compound dilution into each well (f.v. 110 ul) on            duplicate plates        -   Place in 37 degC incubator for 30 min    -   Make lysates        -   Prepare MSD Lysis buffer; for 10 ml add 200 ul protease            inhibitor solution, and 100 ul each of Phosphatase            inhibitors I & II (Keep on ice until ready for use)        -   Remove plates post-incubation, aspirate media with plate            washer, wash 1× with cold PBS, and add 80 ul MSD Lysis            buffer per well; incubate on shaker at 4 degC for ≧30 min        -   Spin cold at 2500 rpm for 10 min; leave plates in 4 degC            centrifuge until ready for use    -   AKT duplex assay        -   Wash plates (4× with 200 ul/well WB in plate washer); tap            plates on paper towel to blot        -   Add 60 ul of lysates/well, incubate on shaker at RT for 1 hr        -   During incubation prepare detection Ab (3 ml/plate; 2 ml WB            and 1 ml blocking solution w/ Ab at 10 nM); repeat wash step            as above        -   Add 25 ul of Ab/well, incubate on shaker at RT for 1 hr;            repeat wash step as above        -   Add 150 ul/well 1× Read Buffer (dilute 4× stock in ddH2O, 20            ml/plate), read immediately    -   Analysis        -   Observe all the data points at each compound concentration.        -   The data point from highest inhibitor concentration must be            equal or greater than 70% of DMSO control.        -   IC50 for duplicate runs must be within 2-fold of each other            (not flagged in summary template).        -   Y min must be greater than zero; if both mins are red            flagged (>35) then compound is listed as inactive            (IC50=>highest dose). If only one min is red flagged, but            still ≦50 then call IC50 as listed.        -   Any data points equal or greater than 30% off the curve will            not be considered.

Cell Growth/Death Assay:

BT474, HCC1954 and T-47D (human breast) were cultured in RPMI-1640containing 10% fetal bovine serum at 37° C. in 5% CO₂ incubator. Cellswere split into T75 flask (Falcon #353136) two to three days prior toassay set up at density which yields approximately 70-80% confluence attime of harvest for assay. Cells were harvested using 0.25% trypsin-EDTA(Sigma #4049). Cell counts were performed on cell suspension usingTrypan Blue exclusion staining. Cells were then plated in 384 well blackflat bottom polystyrene (Greiner #781086) in 48 μl of culture media perwell at 1,000 cells/well. All plates were placed at 5% CO₂, 37° C.overnight and test compounds were added the following day. One plate wastreated with CellTiter-Glo (Promega #G7573) for a day 0 (t=0)measurement and read as described below. The test compounds wereprepared in clear bottom polypropylene 384 well plates (Greiner #781280)with consecutive two fold dilutions. 4 μl of these dilutions were addedto 105 μl culture media, after mixing the solution, 2 μl of thesedilutions were added into each well of the cell plates. The finalconcentration of DMSO in all wells was 0.15%. Cells were incubated at37° C., 5% CO₂ for 72 hours. Following 72 hours of incubation withcompounds each plate was developed and read. CellTiter-Glo reagent wasadded to assay plates using a volume equivalent to the cell culturevolume in the wells. Plates were shaken for approximately two minutesand incubated at room temperature for approximately 30 minutes andchemiluminescent signal was read on the Analyst GT (Molecular Devices)reader. Results were expressed as a percent of the t=0 and plottedagainst the compound concentration. Cell growth inhibition wasdetermined for each compound by fitting the dose response with a 4 or 6parameter curve fit using XLfit software and determining theconcentration that inhibited 50% of the cell growth (gIC50) with the Ymin as the t=0 and Y max as the DMSO control. Value from wells with nocells was subtracted from all samples for background correction.

Additional References:

The compounds of the present invention can also be tested to determinetheir inhibitory activity at PI3Kα, PI3δ, PI3Kβ and PI3Kγ according tothe following references:

For all PI3K isoforms:

-   1. Cloning, expression, purification, and characterization of the    human Class la phosphoinositide 3-kinase isoforms: Meier, T. I.;    Cook, J. A.; Thomas, J. E.; Radding, J. A.; Horn, C.; Lingaraj, T.;    Smith, M. C. Protein Expr. Purif., 2004, 35(2), 218.-   2. Competitive fluorescence polarization assays for the detection of    phosphoinositide kinase and phosphatase activity: Drees, B. E.;    Weipert, A.; Hudson, H.; Ferguson, C. G.; Chakravarty, L.;    Prestwich, G. D. Comb. Chem. High Throughput. Screen., 2003, 6(4),    321.

For PI3Kγ: WO 2005/011686 A1

The pharmaceutically active compounds within the scope of this inventionare useful as PI3 Kinase inhibitors in mammals, particularly humans, inneed thereof.

The present invention therefore provides a method of treating diseasesassociated with PI3 kinase inhibition, particularly: autoimmunedisorders, inflammatory diseases, cardiovascular diseases,neurodegenerative diseases, allergy, asthma, pancreatitis, multiorganfailure, kidney diseases, platelet aggregation, cancer, sperm motility,transplantation rejection, graft rejection and lung injuries and otherconditions requiring PI3 kinase modulation/inhibition, which comprisesadministering an effective compound of Formula (I) or a pharmaceuticallyacceptable salt, hydrate, solvate or pro-drug thereof. The compounds ofFormula (I) also provide for a method of treating the above indicateddisease states because of their ability to act as PI3 inhibitors. Thedrug may be administered to a patient in need thereof by anyconventional route of administration, including, but not limited to,intravenous, intramuscular, oral, subcutaneous, intradermal, andparenteral.

The pharmaceutically active compounds of the present invention areincorporated into convenient dosage forms such as capsules, tablets, orinjectable preparations. Solid or liquid pharmaceutical carriers areemployed. Solid carriers include, starch, lactose, calcium sulfatedihydrate, terra alba, sucrose, talc, gelatin, agar, pectin, acacia,magnesium stearate, and stearic acid. Liquid carriers include syrup,peanut oil, olive oil, saline, and water. Similarly, the carrier ordiluent may include any prolonged release material, such as glycerylmonostearate or glyceryl distearate, alone or with a wax. The amount ofsolid carrier varies widely but, preferably, will be from about 25 mg toabout 1 g per dosage unit. When a liquid carrier is used, thepreparation will be in the form of a syrup, elixir, emulsion, softgelatin capsule, sterile injectable liquid such as an ampoule, or anaqueous or nonaqueous liquid suspension.

The pharmaceutical preparations are made following conventionaltechniques of a pharmaceutical chemist involving mixing, granulating,and compressing, when necessary, for tablet forms, or mixing, fillingand dissolving the ingredients, as appropriate, to give the desired oralor parenteral products.

Doses of the presently invented pharmaceutically active compounds in apharmaceutical dosage unit as described above will be an efficacious,nontoxic quantity preferably selected from the range of 0.001-100 mg/kgof active compound, preferably 0.001-50 mg/kg. When treating a humanpatient in need of a PI3K inhibitor, the selected dose is administeredpreferably from 1-6 times daily, orally or parenterally. Preferred formsof parenteral administration include topically, rectally, transdermally,by injection and continuously by infusion. Oral dosage units for humanadministration preferably contain from 0.05 to 3500 mg of activecompound. Oral administration, which uses lower dosages is preferred.Parenteral administration, at high dosages, however, also can be usedwhen safe and convenient for the patient.

Optimal dosages to be administered may be readily determined by thoseskilled in the art, and will vary with the particular PI3 kinaseinhibitor in use, the strength of the preparation, the mode ofadministration, and the advancement of the disease condition. Additionalfactors depending on the particular patient being treated will result ina need to adjust dosages, including patient age, weight, diet, and timeof administration.

The method of this invention of inducing PI3 kinase inhibitory activityin mammals, including humans, comprises administering to a subject inneed of such activity an effective PI3 kinase modulating/inhibitingamount of a pharmaceutically active compound of the present invention.

The invention also provides for the use of a compound of Formula (I) inthe manufacture of a medicament for use as a PI3 kinase inhibitor.

The invention also provides for the use of a compound of Formula (I) inthe manufacture of a medicament for use in therapy.

The invention also provides for the use of a compound of Formula (I) inthe manufacture of a medicament for use in treating autoimmunedisorders, inflammatory diseases, cardiovascular diseases,neurodegenerative diseases, allergy, asthma, pancreatitis, multiorganfailure, kidney diseases, platelet aggregation, cancer, sperm motility,transplantation rejection, graft rejection and lung injuries.

The invention also provides for a pharmaceutical composition for use asa PI3 inhibitor which comprises a compound of Formula (I) and apharmaceutically acceptable carrier.

The invention also provides for a pharmaceutical composition for use inthe treatment of autoimmune disorders, inflammatory diseases,cardiovascular diseases, neurodegenerative diseases, allergy, asthma,pancreatitis, multiorgan failure, kidney diseases, platelet aggregation,cancer, sperm motility, transplantation rejection, graft rejection andlung injuries, which comprises a compound of Formula (I) and apharmaceutically acceptable carrier.

In addition, the pharmaceutically active compounds of the presentinvention can be co-administered with further active ingredients,including compounds known to have utility when used in combination witha PI3 kinase inhibitor.

Without further elaboration, it is believed that one skilled in the artcan, using the preceding description, utilize the present invention toits fullest extent. The following examples are, therefore, to beconstrued as merely illustrative and not a limitation of the scope ofthe present invention in any way.

Experimental Details

The compounds of the following examples are readily made according toSchemes I-5 or by analogous methods.

Schemes:

Quinoxalines such as represented by compounds of Formula I can beprepared from, for example, bromoquinoxalinols (2) which have beenprepared in the literature (Journal of Medicinal Chemistry, 1981, 24(1),93-101). As outlined in Scheme 1, bromoquinoxalinols such as compound 2may be converted to a bromochloroquinoxaline such as compound 3 by forexample, treatment with phosphorous oxychloride at elevated temperatures(typically 120° C.). The resulting chlorinated compound (3) may undergoa variety of coupling reactions as delineated by steps C, D or E. Whenthe coupling step is for instance a nucleophilic displacement reactionsuch as for steps C or D, suitable nucleophiles such as amines, oralkoxides are commercially available or easily prepared by methods knownto those skilled in the art. In the instances where the coupling step isan amine or alkoxide displacement of the chloride in compound 3, such adisplacement may be carried out at room temperature or furtherfacilitated by heating to temperatures such as 70-100° C. either in neatreagent or in a suitable polar solvent such as N,N′-dimethylformamide.Alternatively, the coupling step to prepare compounds of formula 4 maybe a transition metal (such as palladium) catalyzed cross-couplingreaction of an aryl or heteroaryl stannane, boronate ester or boronicacid with compound 3, such as in step E. An exemplary coupling reactionsuch as a Suzuki cross-coupling depicted in step E can be achieved bytreating compound 3 with an appropriate palladium catalyst (typically1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1)), in the presence of inorganic base (such as potassiumcarbonate, sodium carbonate or sodium bicarbonate) and a suitablesolvent (such as 1,4-dioxane or N,N′-dimethylformamide) at elevatedtemperatures (typically 100° C.). The resulting compounds of formula (4)may undergo another palladium catalyzed coupling reaction as describedabove with an aryl or heteroaryl boronate ester or boronic acid tofurnish compounds of the present invention such as 6. Likewise, in theinstances when R2 in compound 4 is N or O, borylation can be achievedwith a palladium catalyst (such as1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1)) in the presence of base (such as potassium acetate) insolvent (such as dioxane) at elevated temperature (typically 100° C.) toprovide boronate esters such as compound 5. Such boronate esters canundergo typical Suzuki cross-coupling reactions (as described above)with appropriate aryl or heteroaryl halides to provide compounds of thepresent invention, such as compound 6.

Scheme 2 describes the removal of an amine protecting group when it isnecessary to protect an amine before a coupling reaction (such as insteps C, D, or E in Scheme 1 above) can be carried out. For example, aBoc-protected amine such as compound 7 can be treated withtrifluoroacetic acid in a suitable solvent (such as acetonitrile) at rtto furnish compounds of the present invention such as compound 8.

Schemes 3, 4, 5 and 6 describe exemplary preparations of non-commercialintermediate amines, bromides or boronate esters used.

EXPERIMENTAL SECTION

Compounds of the present invention can be prepared according to Scheme1, using different coupling groups in steps C, D, and E. Alternativecoupling groups for step C, D, and E are all commercially available ordescribed in preparations for Intermediates 1, 2, 3, 4, 5 and 6 below.

Exemplary preparations are described in Examples 1, 37 and 43. Allclaimed compounds can be prepared by the preparations described in thissection.

Example 1 Preparation of2-(4-morpholinyl)-7-(1H-pyrazolo[3,4-b]pyridin-5-yl)quinoxaline

a) 7-bromo-2(1H)-quinoxalinone

Prepared according to the procedure described in Journal of MedicinalChemistry, 1981, 24(1), 93-101.

b) 7-Bromo-2-chloroquinoxaline

A slurry of 7-bromo-2(1H)-quinoxalinone (22.2 mmol) in neat phosphorusoxychloride (50 ml) was heated at 120° C. for 20 hours. The reaction wascooled to ambient temperature then concentrated under reduced pressureto a purple residue. The residue was taken into ethyl acetate thenslowly poured into ice-cold, saturated aqueous sodium bicarbonatesolution (˜100 ml) and extracted with ethyl acetate. The extracts werewashed with saturated aqueous sodium bicarbonate and brine then driedover anhydrous sodium sulfate and decolorizing charcoal. The slurry wasfiltered through Celite then concentrated under reduced pressure to givethe title compound (3.0 g, 55%) as a white solid. MS(ES)+ m/e 242.9;244.8 [M+]⁺.

c) 7-Bromo-2-(4-morpholinyl)quinoxaline

A solution of 7-bromo-2-chloroquinoxaline (6.16 mmol) inN,N-dimethylformamide (20 ml) was treated with an amine or alcohol suchas neat morpholine (18.5 mmol) then heated at 80° C. for 1 hour. Thereaction was cooled to ambient temperature then concentrated underreduced pressure to a yellow residue. The residue was taken into ethylacetate and washed with portions of saturated aqueous sodiumbicarbonate. The organic phase was dried over anhydrous sodium sulfateand decolorizing charcoal then filtered through Celite. The filtrate wasconcentrated under reduced pressure to give (1.43 g, 95%) as a yellowsolid. MS(ES)+ m/e 293.7; 295.9 [M+]⁺.

d)2-(4-Morpholinyl)-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline

A slurry of 7-bromo-2-(4-morpholinyl)quinoxaline (0.67 mmol),bis(pinacolato)diboron (0.87 mmol), potassium acetate (1.33 mmol) and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.03 mmol) in anhydrous 1,4-dioxane (10 ml) was heated at110° C. for 18 hours. The reaction mixture was cooled to ambienttemperature then filtered through a short pad of silica (˜15 g) toppedwith anhydrous sodium sulfate (˜5 g), rinsing with ethyl acetate. Thefiltrate was concentrated under reduced pressure to a brown residue thenpurified by column chromatography on silica (15% hexanes in ethylacetate). The desired fractions were combined and concentrated to givethe title compound (186 mg, 81%) as a yellow solid. MS(ES)+ m/e 342.0[M+]⁺.

e) 2-(4-Morpholinyl)-7-(1H-pyrazolo[3,4-b]pyridin-5-yl)quinoxaline

A slurry of2-(4-morpholinyl)-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline(0.56 mmol), a heteroaryl bromide such as5-bromo-1H-pyrazolo[3,4-b]pyridine (0.47 mmol),[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.05 mmol) and 2 M aqueous sodium carbonate (1.88 mmol)in 1,4-dioxane (5 ml) was heated at 110° C. for 18 hours. The reactionwas cooled to ambient temperature then filtered through a short pad ofsilica (˜15 g) topped with anhydrous sodium sulfate (˜5 g), rinsing wellwith ethyl acetate. The filtrate was concentrated under reduced pressureto a brown residue then purified by column chromatography on silica (10%hexanes in ethyl acetate). The desired fractions were combined andconcentrated to give the title compound (40 mg, 26%) as a light yellowsolid. MS(ES)+ m/e 333.1 [M+H]⁺.

The following compounds were or can be prepared following the proceduresused to prepare Example 1:

MS(ES) Example Structure [M + H]⁺ 2

323 3

420 4

332 5

332 6

293 7

293 8

323 9

263 10

402 11

415 12

442 13

372 14

346 15

458 16

430 17

403 18

403 19

373 20

427 21

407 22

448 23

369 24

386 25

399 26

471 27

372 28

459 29

413 30

415 31

465 32

484 33

441 34

358 35

525 36

495 37

463 38

412 39

539 40

484 41

531 42

511 43

497 44

495 45

461 46

497 47

320 48

475 49

503 50

517 51

429 52

496 53

464 54

489 55

461 56

489 57

527 58

449 59

513 60

435 61

499 62

539 63

475 64

568 65

631 66

391 67

390 68

331

Example 69 Preparation of2-amino-N,N-dimethyl-5-[3-(4-pyridinyl)-6-quinoxalinyl]-3-pyridinesulfonamide

a) 7-bromo-2-(4-pyridinyl)quinoxaline

A mixture of 7-bromo-2-chloroquinoxaline (2.05 mmol), pyridine-4-boronicacid (2.05 mmol),[1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.1025 mmol), 2M aqueous potassium carbonate (5 mL) andanhydrous 1,4-dioxane (15 mL) was heated at 100° C. for 16.5 h in asealed pressure vessel. After cooling to room temperature, the organiclayer was separated and purified directly on silica gel, eluting with50-100% ethyl acetate in hexanes to provide the title compound as ayellow solid (382 mg, 65% yield). MS(ES)+ m/e 285.9; 287.8 [M+]⁺.

b)2-amino-N,N-dimethyl-5-[3-(4-pyridinyl)-6-quinoxalinyl]-3-pyridinesulfonamide

A mixture of 7-bromo-2-(4-pyridinyl)quinoxaline (0.245 mmol),2-amino-N,N-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinesulfonamide(0.245 mmol),[1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.0196 mmol), 2M aqueous potassium carbonate (2 mL) andanhydrous 1,4-dioxane (6 mL) was heated at 100° C. for 4 h in a sealedpressure vessel. After cooling to room temperature, the organic layerwas separated and purified directly on silica gel, eluting with 0-10%methanol in ethyl acetate followed by a second purification by HPLC(eluting with acetonitrile: 0.1% TFA in H₂O) to afford the titlecompound as a bright yellow solid (47 mg, 47% yield). MS(ES)+ m/e 407.2[M+H]⁺.

The following compounds were or can be prepared following the proceduresused to prepare Example 69:

MS(ES) Compound Structure [M + H]⁺ 70

364 71

364 72

363 73

324 74

408 75

420 76

456 77

440 78

440 79

441

Example 80 Preparation of5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinesulfonamide

A solution of 1,1-dimethylethyl4-{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}-1-piperazinecarboxylate(0.21 mmol) (prepared according to Scheme 1) in acetonitrile (4 mL) wastreated with concentrated trifluoroacetic acid (4 mL) for 2 hours. Thereaction mixture was then concentrate and neutralized with saturatedsodium bicarbonate (20 mL) and extracted with ethyl acetate (3×20 mL).The combined organic layers were washed with brine, dried over sodiumsulfate, filtered and concentrated to yield the title product. MS(ES)+m/e 371.0 [M+H]⁺.

*Similar compounds were or can be prepared following the procedures usedto prepare Example 80, with or without N,N′-dimethylformamide assolvent.

Example 81 Preparation ofN-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

a) 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxaline

A slurry of 7-bromo-2-chloroquinoxaline (10.0 mmol),1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole(10.5 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.3 mmol) in 2M aqueous potassium carbonate (15 mL) and1,4-dioxane (40 mL) was heated at 100° C. for 4 h. The reaction mixturewas cooled, poured into water (100 mL), and extracted with (3×100 mL)ethyl acetate. The combined organic layers were filtered through a padof Celite while rinsing with water and ethyl acetate. The filtrate wasseparated and the organic layer was dried over sodium sulfate, filtered,and concentrated in vacuo. Purification of the residue by silica gelchromatography (40-70% ethyl acetate/hexanes) provided the titlecompound as a yellow solid (1.73 g, 57%). MS(ES)+ m/e 289, 291 [M+H]⁺.

b)N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

A mixture of 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxaline (5.98mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(6.78 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.18 mmol) in 2M aqueous sodium carbonate (15 mL) and1,4-dioxane (40 mL) was heated at 100° C. for 22 h. AdditionalN-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.83 mmol),[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.09 mmol), and 2M aqueous potassium carbonate (3 mL)were added and the reaction mixture was heated at 100° C. for 22 h forcomplete consumption of starting material. The reaction mixture wascooled, diluted with diethyl ether (30 mL), and filtered through a padof Celite while rinsing with (2×30 mL) diethyl ether. The organic layerwas poured into a separatory funnel containing water (100 mL) and thelayers were separated. The aqueous layer was acidified with 6N aqueousHCl until the pH was approximately 7 and then further extracted with(3×200 mL) ethyl acetate. The combined organic layers were dried oversodium sulfate with decolorizing activated carbon, filtered through apad of Celite while rinsing with (2×100 mL) ethyl acetate, andconcentrated in vacuo. The filtrate was separated and the organic layerwas dried over sodium sulfate, filtered, and concentrated in vacuo.Recrystallization of the residue from hot ethyl acetate afforded thetitle product as an ivory solid (804 mg, 30%). Additional product wasobtained from the concentrated mother liquors after purification bysilica gel chromatography (70-100% ethyl acetate/hexanes) followed byprecipitation from cold ethyl acetate (534 mg, 20%). MS(ES)+ m/e 443[M+H]⁺.

* Related analogs such as the following were or can be preparedfollowing the general procedures in Example 81 by varying the choice ofboronate ester and heteroaryl halide coupling partners. Some analogscould be isolated by direct purification of the organic layer byalternative purification methods such as reverse phase Gilson HPLC,silica gel chromatography, recrystallization from ethanol, ortrituration from other solvents.

MS(ES) Example Structure [M + H]⁺ 82

353 83

353 84

536 85

429 86

500 87

457 88

473 89

443 90

471 91

458 92

485 93

542 94

569 95

429 96

487 97

443 98

514 99

479 100

486 101

303 102

457 103

457 104

442 105

478 106

409 107

447 108

461 109

531 110

517 111

473 112

514 113

437 114

509 115

411 116

493 117

421 118

491

Example 119 Preparation of2,4-difluoro-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

A mixture of2-(1-methyl-1H-pyrazol-4-yl)-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline(9.22 mmol), N-(5-bromo-3-pyridinyl)-2,4-difluorobenzenesulfonamide(8.13 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.404 mmol) in 2M aqueous sodium carbonate (40 mL) and1,4-dioxane (40 mL) was heated at 100° C. for 1 h. Upon cooling, thereaction mixture separated into two layers (aqueous and organic). Theorganic layer was partitioned between ethyl acetate (50 mL) and water(25 mL). The two aqueous layers were then combined and the pH wasadjusted to ˜7 with 2N aqueous HCl. A solid precipitated and wasfiltered away from the solution. The solid was dried in vacuo and thendesiccated over P₂O₅ to afford the title product (2.5 g, 64%). MS(ES)+m/e 479 [M+H]⁺.

Example 120 Preparation of4-cyano-N-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

To a solution of5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinamine (52 g,0.172 mmol) in pyridine (1.7 mL) was added 4-cyanobenzenesulfonylchloride (56 mg, 0.278 mmol). The reaction mixture was stirred at roomtemperature overnight. Monitoring by LCMS still showed 30% of startingmaterial. An additional portion of 4-cyanobenzenesulfonyl chloride (17mg, 0.084 mmol) was added to the reaction mixture and after stirring fora further 30 minutes, all starting material was consumed. Cold water waspoured into the reaction resulting in precipitate formation. This solidwas collected by filtration, washed with water and dried under vacuum togive the title compound (54 mg, 67%) as a brown colored solid. MS(ES)+m/e 468 [M+H]⁺.

The following compounds were or can be prepared following the generalprocedures used to prepare the compound of Example 120 above:

MS(ES) Compound Structure [M + H]⁺ 121

381 122

461 123

461 124

407 125

447 126

409 127

463 128

529 129

449 130

462 131

475 132

395 133

423 134

461 135

423 136

449 137

473 138

461 139

457 140

503 141

471 142

485 143

485 144

472 145

503 146

511 147

449 148

491 149

475 150

475 151

511 152

511 153

496 154

512 155

512 156

449 157

478 158

473 159

496 160

553 161

546 162

536 163

536 164

550 165

510 166

521 167

535 168

554 169

591 170

565 171

526 172

540 173

615 174

599 175

501 176

585 177

641 178

479 179

423 180

492 181

478 182

478 183

485

Example 184 Preparation ofN-{5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinyl}acetamide

A solution of5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinamine (0.46 mmol)in pyridine (3 ml) was treated with a sulfonyl chloride, acyl chlorideor anhydride such as acetic anhydride (0.56 mmol) and heated at 50° C.for 18 hour. The reaction mixture was treated with another portion ofacetic anhydride (0.10 mmol) and stirred for another 2 days. Thereaction mixture was diluted with water and saturated sodium bicarbonate(aq) and extracted with ethyl acetate. The ethyl acetate layer was driedover Na₂SO₄ filtered and concentrated under reduced pressure. Theresidue was taken into hot ethyl acetate and diluted with hexanes andcool to 0° C. The reaction mixture was filtered and washed with hexanesto give the title compound (98 mg, 58%) MS(ES)+ m/e 321 [M+H]⁺.

The following compounds were or can be prepared following the proceduresused to prepare Example 184 using the appropriate sulfonyl chloride,anhydride or acyl chloride:

Example Structure MS(ES) [M + H]⁺ 185

363 186

461 187

399 188

477

Example 189 Preparation ofN,N-dimethyl-N′-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}sulfamide

In an oven dried high pressure vessel under a nitrogen atmosphere,7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxaline (150 mg, 0.519 mmol),bis(pinacolato)diboron (158 mg, 0.623 mmol), potassium acetate (153 mg,1.556 mmol), and1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloridedichloromethane complex (18.98 mg, 0.026 mmol) in anhydrous 1,4-dioxane(2 mL) was stirred at 100° C. in an oil bath for 1 hr. The reactionmixture was cooled to room temperature.N′-(5-bromo-3-pyridinyl)-N,N-dimethylsulfamide (145 mg, 0.519 mmol)followed by sodium bicarbonate (131 mg, 1.556 mmol) in water (0.67 mL)were added to the reaction mixture and the vessel was sealed again. Thereaction was stirred at 100° C. for 16.75 hours then cooled to roomtemperature. The reaction was filtered through Celite and the pad waswashed with ethyl acetate. The bi-phasic mixture was separated in aseparatory funnel. The organic layer was washed with brine (20 mL),dried over magnesium sulfate, and concentrated in vacuo to give a brownsolid. Trituration of the brown solid in dichloromethane (3 drops) andether (8 mL) provided the title compound (120 mg, 57%) as a light brownsolid. MS(ES)+ m/e 410.2 [M+H]⁺.

Example 190 Preparation ofN-{5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinyl}-4-morpholinesulfonamide

In an oven-dried flask under nitrogen, a solution of5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinamine (99 mg,0.327 mmol) in pyridine (3 mL) at room temperature was treated withmorpholine-4-sulfonyl chloride (96 mg, 0.491 mmol) by syringe. Thereaction was stirred at room temperature for 16.5 hours. The reactionwas very sluggish so the reaction was placed in an oil bath at 50° C.and stirred at that temperature for 23 hours. The reaction wasprogressing to the desired product as determined by LCMS but was not yetcomplete. The reaction mixture was stirred for an additional 4 days at50° C. The reaction did not progress to completion. The reaction wascooled to room temperature and concentrated in vacuo. The residue wastaken up into 200 mL ethyl acetate and 50 mL water. The organic layerwas washed with saturated aqueous sodium bicarbonate solution (100 mL)followed by brine (100 mL), dried over magnesium sulfate andconcentrated in vacuo. Purification by silica gel chromatography elutingwith 0-10% methanol in dichloromethane provided the desired product as aresidue which was not pure. Addition of dichloromethane/ether resultedin precipitate formation. The precipitate was collected by filtration.Recrystallization of the precipitate from ethanol provided the titlecompound (26 mg, 18%) as a rust-coloured solid. MS(ES)+ m/e 452.0[M+H]⁺.

Related sulfamide analogs can be prepared in a similar manner using theappropriate sulfamoyl chloride.

Example 191 Preparation of2-phenyl-N-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)acetamide

a) N-(7-bromo-2-quinoxalinyl)-2-phenylacetamide

A slurry of 7-bromo-2-chloroquinoxaline (0.493 mmol), 2-phenylacetamide(0.518 mmol), cesium carbonate (0.739 mmol),(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane) (XantPhos,0.029 mmol), and palladium(II)acetate (0.018 mmol) in 1,4-dioxane (3 mL)was heated at 100° C. for 18 h. The reaction mixture was cooled, pouredinto water (50 mL) and brine (20 mL), and extracted with ethyl acetate(3×50 mL). The combined organic layers were dried over sodium sulfate,filtered, and concentrated in vacuo. Purification of the residue bysilica gel chromatography (10-30% ethyl acetate/hexanes) provided thetitle compound as a yellow solid (90 mg, 51%). MS(ES)+ m/e 342, 344[M+H]⁺.

b)2-phenyl-N-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)acetamide

A mixture of N-(7-bromo-2-quinoxalinyl)-2-phenylacetamide (0.254 mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.508 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethane complex (1:1) (0.007 mmol) in 2M aqueous sodiumcarbonate (0.5 mL) and 1,4-dioxane (2 mL) was heated at 100° C. for 5 h.The reaction mixture was cooled, poured into water (60 mL) and brine (15mL), and extracted with ethyl acetate (50 mL). The aqueous layer wasacidified with 1N aqueous HCl until the pH was approximately 6-7 andthen further extracted with (3×50 mL) ethyl acetate. The combinedorganic layers were dried over sodium sulfate, filtered, andconcentrated in vacuo. Purification of the residue by silica gelchromatography eluting with 50-70% ethyl acetate/hexanes followed byreverse phase HPLC (30-75% acetonitrile/water with 0.1% TFA) affordedthe title product as a tan solid (42 mg, 33%). MS(ES)+ m/e 496 [M+H]⁺.

The following compounds were or can be prepared in a similar manner tothe compound of Example 191 using the appropriate amide or sulfonamide:

Example Structure MS(ES) [M + H]⁺ 192

482 193

518

Example 194 Preparation of1,1-dimethylethyl[2-(4-{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}-1-piperazinyl)ethyl]carbamate

a)1,1-dimethylethyl{2-[4-(7-bromo-2-quinoxalinyl)-1-piperazinyl]ethyl}carbamate

A solution of 7-bromo-2-chloroquinoxaline (1.20 mmol) inN,N-dimethylformamide (5 ml) was treated with an amine (or an alcohol)such as 1,1-dimethylethyl[2-(1-piperazinyl)ethyl]carbamate (3.60 mmol)then heated at 80° C. for 1 hour. The reaction was cooled to ambienttemperature then poured into water (25 ml). Product precipitated out ofsolution, which was filtered and dried. Alternatively, after thereaction is cooled to ambient temperature and poured into water (25 ml),it was extracted into ethyl acetate (3×25 ml). The extracts were washedwith brine then dried over anhydrous sodium sulfate, filtered andconcentrated under reduced pressure to give the title compound (520 mg,80%) as a yellow solid. MS(ES)+ m/e 297.2 [M+]⁺.

b)1,1-dimethylethyl[2-(4-{7-[5-(aminosulfonyl)-3-pyridinyl]-2-quinoxalinyl}-1-piperazinyl)ethyl]carbamate

A slurry of 1,1-dimethylethyl{2-[4-(7-bromo-2-quinoxalinyl)-1-piperazinyl]ethyl}carbamate (0.96mmol), bis(pinacolato)diboron (1.06 mmol), potassium acetate (3.84mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.07 mmol) in 1,4-dioxane (5 ml) was heated at 100° C.After the reaction stirred for 1 hour, 5-bromo-3-pyridinesulfonamide(0.96 mmol) and 2M potassium carbonate (aq) (4 ml) was added and thereaction mixture stirred for 18 hours. The reaction was cooled toambient temperature, separated the organic layer and purified directlyon silica by column chromatography (10% ethyl acetate/hexanes). Thedesired fractions were combined and concentrated to give the titlecompound (20 mg, 7%) as a light yellow solid. MS(ES)+ m/e 514.2 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 195 using the appropriate amine (or alcohol):

Example Structure MS(ES) [M + H]⁺ 196

374 197

402 198

477 199

489 200

447 201

462 202

477 203

436

Example 204 Preparation ofN-(2,4-difluorophenyl)-5-{3-[4-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinesulfonamide

a) 1-(7-bromo-2-quinoxalinyl)-N,N-dimethyl-4-piperidinamine

A solution of 7-bromo-2-chloroquinoxaline (1.20 mmol) inN,N-dimethylformamide (5 ml) was treated with an amine (or an alcohol)such as 1,1-dimethylethyl[2-(1-piperazinyl)ethyl]carbamate (3.60 mmol)then heated at 80° C. for 1 hour. The reaction was cooled to ambienttemperature then poured into water (25 ml). Product precipitated out ofsolution, which was filtered and dried. Alternatively, after thereaction is cooled to ambient temperature and poured into water (25 ml),it was extracted into ethyl acetate (3×25 ml). The extracts were washedwith brine then dried over anhydrous sodium sulfate, filtered andconcentrated under reduced pressure to give the title compound (400 mg,99%) as a yellow solid. MS(ES)+ m/e 336.2 [M+]⁺.

b)N-(2,4-difluorophenyl)-5-{3-[4-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinesulfonamide

A slurry of 1-(7-bromo-2-quinoxalinyl)-N,N-dimethyl-4-piperidinamine(1.2 mmol), bis(pinacolato)diboron (1.30 mmol), potassium acetate (4.80mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.09 mmol) in 1,4-dioxane (5 ml) was heated at 100° C.After the reaction stirred for 2.5 hours, 5-bromo-3-pyridinesulfonamide(0.96 mmol) and 2M solution potassium carbonate (5 ml) was added andcontinued to stir for 18 hours. The reaction was cooled to ambienttemperature, separated the organic layer and purified directly on silicaby column chromatography (5%, 5% ammonium hydroxide/methanol:ethylacetate). The desired fractions were combined and concentrated to givethe title compound (20 mg, 3%) as a tan solid. MS(ES)+ m/e 525.2 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 204 using the appropriate amine or phenol. In some cases,pretreatment of the amine with sodium hydride (3 equivalents) wasrequired:

Example Structure MS(ES) [M + H]⁺ 205

689 206

525.2 207

442 208

504 209

491 210

577 211

574 212

574

Example 213 Preparation ofN-(2-chloro-5-{3-[3-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

a) 1-(7-bromo-2-quinoxalinyl)-N,N-dimethyl-3-piperidinamine

A solution of 7-bromo-2-chloroquinoxaline (1.20 mmol) inN,N-dimethylformamide (5 ml) was treated with an amine (or an alcohol)such as N,N-dimethyl-3-piperidinamine dihydrochloride (3.60 mmol) andtriethylamine (7.20 mmol) then heated at 100° C. for 1 hour. Thereaction was cooled to ambient temperature then poured into water (25ml). Product precipitated out of solution, which was filtered and dried.Alternatively, after the reaction is cooled to ambient temperature andpoured into water (25 ml), it was extracted into ethyl acetate (3×25ml). The extracts were washed with brine then dried over anhydroussodium sulfate, filtered and concentrated under reduced pressure to givethe title compound (400 mg, 99%) as an orange solid. MS(ES)+ m/e 336.2[M+]⁺.

b) Preparation ofN-(2-chloro-5-{3-[3-(dimethylamino)-1-piperidinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

A slurry of 1-(7-bromo-2-quinoxalinyl)-N,N-dimethyl-3-piperidinamine(1.2 mmol), bis(pinacolato)diboron (1.30 mmol), potassium acetate (4.80mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.09 mmol) in 1,4-dioxane (5 ml) was heated at 100° C.After the reaction stirred for 2.5 hours,N-(5-bromo-2-chloro-3-pyridinyl)benzenesulfonamide (1.20 mmol) and 2Msolution potassium carbonate (5 ml) was added and continued to stir for18 hours. The reaction was cooled to ambient temperature, concentrated,redissolved in methanol and purified on reverse phase HPLC (0.1%trifluoracetic acid/water in acetonitrile). The desired fractions werecombined, neutralized with saturated sodium bicarbonate, extracted withethyl acetate (3×20 ml). Combined organic layers were washed with brine,dried over sodium sulfate, filtered and concentrated to give the titlecompound (52 mg, 10%) as a yellow solid. MS(ES)+ m/e 524.2 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 213 using the appropriate amine:

Example Structure MS(ES) [M + H]⁺ 214

488 215

496 216

524 217

538 218

510 219

489 220

494 221

581 222

558 223

600 224

589 225

424 226

495 227

582 228

651

Example 229 Preparation ofN-{2-chloro-5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

To a solution of 1,1-dimethylethyl4-(7-{6-chloro-5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate(0.83 mmol) in acetonitrile (6 ml) was added concentratedtrifluoroacetic acid (3 ml). The reaction stirred at ambient temperaturefor 3 hours and was then concentrated to an orange oil. The residue wasneutralized with saturated sodium bicarbonate solution upon which aprecipitate was formed. The product was filtered and dried to give thetitle compound (260 mg, 65%) as an off-white solid. MS(ES)+ m/e 481.2[M+H]⁺.

Example 230 Preparation ofN-(2-chloro-5-{3-[4-(methylsulfonyl)-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

To a solution ofN-{2-chloro-5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide(0.23 mmol), triethylamine (0.92 mmol), in dichloromethane (5 ml) wasadded methanesulfonyl chloride (0.25 mmol), which stirred at 50° C. for18 hours. The reaction was cooled to ambient temperature, concentrated,redissolved in methanol and purified on reverse phase HPLC (0.1%ammonium hydroxide/water in acetonitrile). The desired fractions werecombined and concentrated to give the title compound (7.8 mg, 2%) as awhite solid. MS(ES)+ m/e 560.2 [M+H]⁺.

Example 231 Preparation ofN-[5-(3-{4-[2-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide

a) 7-bromo-2-{4-[2-(methyloxy)phenyl]-1-piperazinyl}quinoxaline

A solution of 7-bromo-2-chloroquinoxaline (1.20 mmol) inN,N-dimethylformamide (15 ml) was treated with an amine (or an alcohol)such as 1-[2-(methyloxy)phenyl]piperazine (3.60 mmol) and then heated at100° C. for 1 hour. The reaction was cooled to ambient temperature thenpoured into water (25 ml) and extracted into ethyl acetate (3×25 ml).The extracts were washed with brine then dried over anhydrous sodiumsulfate, filtered, concentrated and the residue crystallized with ethylacetate:hexanes to give the title compound (331 mg, 70%) as yellowcrystals. MS(ES)+ m/e 398.2 [M+]⁺.

b)N-[5-(3-{4-[2-(methyloxy)phenyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide

A slurry of a boronate ester such asN-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.55 mmol),7-bromo-2-{4-[2-(methyloxy)phenyl]-1-piperazinyl}quinoxaline (0.37mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.03 mmol) in 1,4-dioxane (4 ml) and 2M potassiumcarbonate (aq) (2 ml) was stirred at 100° C. for 18 hours. The reactionwas cooled to ambient temperature, the organic layer separated andpurified directly on silica by column chromatography (80% ethylacetate/hexanes). The desired fractions were combined and concentratedto give the title compound (99 mg, 48%) as a yellow solid. MS(ES)+ m/e553.4 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 231 using the appropriate amine:

Example Structure MS(ES) [M + H]⁺ 232

448 233

538 234

553 235

538 236

460 237

553 238

617 239

581 240

544 241

496 242

525 243

567 244

547 245

538 246

538 247

591 248

531 249

546 250

665 251

694 252

603 253

596 254

629 255

602 256

672 257

630 258

581 259

647 260

616 261

654 262

616 263

728 264

717 265

547 266

644 267

560 268

584 269

658

Example 270 Preparation ofN-(5-{3-[(1-methyl-1H-pyrazol-3-yl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

a) 7-bromo-N-(1-methyl-1H-pyrazol-3-yl)-2-quinoxalinamine

A slurry of 7-bromo-2-chloroquinoxaline (1.20 mmol),1-methyl-1H-pyrazol-3-amine (2.50 mmol), potassium t-butoxide (2.50mmol) in 1,4-dioxane (5 ml) was stirred at 100° C. for 30 minutes in theSmith Synthesizer microwave reactor. The reaction was poured into water(25 ml) upon which a precipitate formed, which was filtered and dried toafford the title compound (250 mg, 67%) as a yellow solid. MS(ES)+ m/e303.9 [M+H]⁺.

b)N-(5-{3-[(1-methyl-1H-pyrazol-3-yl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

A slurry of 7-bromo-N-(1-methyl-1H-pyrazol-3-yl)-2-quinoxalinamine (0.37mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.55 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.03 mmol) in 1,4-dioxane (4 ml) and 2M solutionpotassium carbonate (2 ml) was stirred at 100° C. for 2 hours. Thereaction was cooled to ambient temperature, separated the organic layerand purified directly on silica by column chromatography (10%methanol/ethyl acetate). The desired fractions were combined andconcentrated to give the title compound (81 mg, 32%) as a pale greensolid. MS(ES)+ m/e 458.1 [M+H]⁺.

The following compound was prepared following the procedures in Example270 using the appropriate amine:

Example Structure MS(ES) [M + H]⁺ 271

458

Example 272 Preparation ofN-{5-[3-(4-{[2-(methylsulfonyl)ethyl]amino}-1-piperidinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

a)1-(7-bromo-2-quinoxalinyl)-N-[2-(methylsulfonyl)ethyl]-4-piperidinamine

A slurry of 1-(7-bromo-2-quinoxalinyl)-4-piperidinone (0.98),2-(methylsulfonyl)ethanamine (2.90 mmol), sodium triacetoxyborohydride(2.90 mmol), triethylamine (1.90 mmol) stirred in a solution ofdichloromethane (4 ml) and acetic acid (1 ml) for 18 hours at ambienttemperature. The reaction was concentrated and then triturated withethyl acetate:hexanes (1:1) which was filtered and dried to give thetitle compound (210 mg, 52%) as a white solid. MS(ES)+ m/e 415.1 [M+H]⁺.

b)N-(5-{3-[(1-methyl-1H-pyrazol-3-yl)amino]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

A slurry of a1-(7-bromo-2-quinoxalinyl)-N-[2-(methylsulfonyl)ethyl]-4-piperidinamine(0.48 mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.53 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.03 mmol) in 1,4-dioxane (4 ml) and 2M solutionpotassium carbonate (2 ml) was stirred at 100° C. for 3 hours. Thereaction was cooled to ambient temperature, separated the organic layerand purified directly on silica by column chromatography (10%methanol/ethyl acetate). The desired fractions were combined andconcentrated to give the title compound (15 mg, 6%) as a tan solid.MS(ES)+ m/e 567.4 [M+H]⁺.

Example 273 Preparation ofN-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

To a solution of 1,1-dimethylethyl4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate(1.80 mmol) in acetonitrile (4 ml) was added concentratedtrifluoroacetic acid (4 ml). The reaction stirred at ambient temperaturefor 18 hours and was then concentrated to an orange oil. The residue wasneutralized with 10% sodium carbonate solution and purified on silica bycolumn chromatography (15% methanol/ethyl acetate). The desiredfractions were combined and concentrated to give the title compound (500mg, 61%) as a tan solid. MS(ES)+ m/e 447.2 [M+H]⁺.

Example 274 Preparation ofN-[5-(3-{4-[(2-methylpropyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide

To a solution ofN-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide(0.20 mmol) and triethylamine (0.20 mmol) in dichloromethane (2 ml) wasadded a sulfonyl chloride such as 2-methyl-1-propanesulfonyl chloride(0.22 mmol). The reaction stirred for 18 hours at ambient temperatureand purified on silica by column chromatography (80% ethylacetate/hexanes). The desired fractions were combined and concentratedto give the title compound (22 mg, 20%) as an off-white solid. MS(ES)+m/e 567.3 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 274 using the appropriate sulfonyl chloride:

Example Structure MS(ES) [M + H]⁺ 275

664 276

593 277

554 278

551

Example 279 Preparation of3-[(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)amino]benzoicacid

a) 3-[(7-bromo-2-quinoxalinyl)amino]-5-(methyloxy)benzoic acid

A slurry of 7-bromo-2-chloroquinoxaline (1.20 mmol) and an aniline suchas 3-aminobenzoic acid (3.70 mmol) in a polar solvent such asdimethylsulfoxide (5 ml) was stirred for 2 hours at 120° C. The reactionwas poured into ice-water upon which a precipitate formed. Theprecipitate was filtered and dried to afford the title compound (400 mg,94%) as a yellow solid. MS(ES)+ m/e 345.8 [M+H]⁺.

b)3-[(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)amino]benzoicacid

A slurry of 3-[(7-bromo-2-quinoxalinyl)amino]-5-(methyloxy)benzoic acid(0.73 mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.80 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.06 mmol) in 1,4-dioxane (4 ml) and 2M solutionpotassium carbonate (2 ml) was stirred at 100° C. for 18 hours. Thereaction was cooled to ambient temperature, separated the organic layerand purified directly on silica by column chromatography (100% ethylacetate). The desired fractions were combined and concentrated to givethe title compound (60 mg, 16%) as a yellow solid. MS(ES)+ m/e 497.8[M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 279 using the appropriate aniline. Alternatively, in someinstances, the aniline in step a was or can be pretreated with 3equivalents of sodium hydride in a solvent such as N,N-dimethylformamideprior to reaction with 7-bromo-2-chloroquinoxaline:

Example Structure MS(ES) [M + H]⁺ 280

483 281

527 282

542 283

329 284

514 285

519

Example 286 Preparation ofN-{5-[3-(2-furanyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

A slurry of 7-bromo-2-chloroquinoxaline (0.82 mmol), a boronic acid suchas 2-furan boronic acid (0.82 mmol),[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.06 mmol), in 1,4-dioxane (4 ml) and 2M solutionpotassium carbonate (2 ml) was stirred at 100° C. for 3 hour. ThenN-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.90 mmol) was added and the reaction mixture stirred at 100° C. for 18hours. The reaction was cooled to ambient temperature, the organic layerseparated and purified directly on silica by column chromatography (50%ethyl acetate/hexanes). The desired fractions were combined andconcentrated to give the title compound (50 mg, 14%) as a tan solid.MS(ES)+ m/e 429.0 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 286 using the appropriate boronic acid, boronate ester orstannane reagent:

Example Structure MS(ES) [M + H]⁺ 287

443 288

443 289

430 290

439 291

446 292

519

Example 293 Preparation of 1,1-dimethylethyl3-oxo-4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate

a) 1,1-dimethylethyl4-(7-bromo-2-quinoxalinyl)-3-oxo-1-piperazinecarboxylate

A slurry of 7-bromo-2-chloroquinoxaline (6.20 mmol), 1,1-dimethylethyl3-oxo-1-piperazinecarboxylate (7.4 mmol), (0.06 mmol), Xantphos (0.28mmol), cesium carbonate (9.20 mmol) in 1,4-dioxane (30 ml) was stirredat 100° C. for 18 hour. The reaction was cooled to ambient temperature,filtered through a pad of celite and purified directly on silica bycolumn chromatography (50% ethyl acetate/hexanes). The desired fractionswere combined and concentrated to give the title compound (1.3 g, 50%)as a yellow solid. MS(ES)+ m/e 409.2 [M+H]⁺.

b) 1,1-dimethylethyl3-oxo-4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate

A slurry of 1,1-dimethylethyl4-(7-bromo-2-quinoxalinyl)-3-oxo-1-piperazinecarboxylate (1.30 mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(1.35 mmol),[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.10 mmol), in 1,4-dioxane (6 ml) and saturated sodiumbicarbonate solution (2 ml) was stirred at 100° C. for 1 hour. Thereaction was cooled to ambient temperature, separated the organic layerand purified directly on silica by column chromatography (80% ethylacetate/hexanes). The desired fractions were combined and concentratedto give the title compound (150 mg, 22%) as a tan solid. MS(ES)+ m/e561.1 [M+H]⁺.

Example 294 Preparation ofN-{5-[3-(2-oxo-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide

To a solution of 1,1-dimethylethyl3-oxo-4-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-1-piperazinecarboxylate(0.21 mmol) in acetonitrile (4 ml) was added concentratedtrifluoroacetic acid (4 ml). The reaction stirred at ambient temperaturefor 1 hour and was then concentrated to an orange oil. The residue wasneutralized with saturated sodium bicarbonate solution upon which aprecipitate formed. The precipitate was dissolved in ethyl acetate andcrashed out of solution with hexanes, which was filtered and dried toafford the title compound (66 mg, 67%) as an off-white solid. MS(ES)+m/e 461.2 [M+H]⁺.

Example 295 Preparation ofN-(5-{3-[4-(methylsulfonyl)-2-oxo-1-piperazinyl]-6-quinoxalinyl}-3-pyridinyl)benzenesulfonamide

a) 1-(7-bromo-2-quinoxalinyl)-2-piperazinone

To a solution of 1,1-dimethylethyl4-(7-bromo-2-quinoxalinyl)-3-oxo-1-piperazinecarboxylate (1.45 mmol) inacetonitrile (10 ml) was added concentrated trifluoroacetic acid (10ml). The reaction stirred at ambient temperature for 1 hour and was thenconcentrated to an orange oil. The residue was neutralized withsaturated sodium bicarbonate solution and extracted into ethyl acetate(3×10 ml). The combined organic layers were washed with brine, driedover sodium sulfate, filtered, and concentrated. The product was thenpurified on silica by column chromatography (20% methanol/ethylacetate). The desired fractions were combined and concentrated to givethe title compound (450 mg, 60%) as a white solid. MS(ES)+ m/e 309.1[M+H]⁺.

b) 1-(7-bromo-2-quinoxalinyl)-4-(methylsulfonyl)-2-piperazinone

To a solution of 1-(7-bromo-2-quinoxalinyl)-2-piperazinone (0.48 mmol)and triethylamine (1.45 mmol), in dichloromethane (5 ml) was added asulfonyl chloride such as methylsulfonyl chloride (1.45 mmol). Thereaction stirred for 3 hours at ambient temperature and then poured intowater (10 ml) and extracted with ethyl acetate (3×20 ml). The combinedorganic layers were washed with brine, dried over sodium sulfate,filtered and concentrated to give the title compound (200 mg, 96%) as awhite solid. MS(ES)+ m/e 384.9 [M+H]⁺.

The following compound was prepared following the procedures in Example295 using the appropriate sulfonyl chloride:

Example Structure MS(ES) [M + H]⁺ 296

631

Example 297 Preparation ofN-{5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide

a)7-bromo-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxaline

To a solution of 7-bromo-2-(1-piperazinyl)quinoxaline (3.41 mmol) inpyridine (20 ml) was added 2-(methyloxy)benzenesulfonyl chloride (10.23mmol). The reaction stirred for 18 hours at 50° C. The reaction wascooled to ambient temperature and a yellow precipitate was filtered andtriturated with methanol to afford the title compound (1.16 g, 73%yield) as a pale yellow solid. MS(ES)+ m/e 463.0 [M+H]⁺.

b)N-{5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide

A slurry of7-bromo-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxaline(0.96 mmol), bis(pinacolato)diboron (0.54 mmol), potassium acetate (1.16mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethane complex (1:1) (0.05 mmol) in 1,4-dioxane (4 ml) washeated at 100° C. After the reaction stirred for 1 hour, a bromide suchas N-(5-bromo-3-pyridinyl)cyclopropanesulfonamide (0.54 mmol) and 2Msolution potassium carbonate (4 ml) was added and continued to stir for1 hour. The reaction was cooled to ambient temperature, separated theorganic layer and purified directly on silica by column chromatography(80% ethyl acetate/hexanes). The desired fractions were combined andconcentrated to give the title compound (44 mg, 14% yield) as a paleyellow solid. MS(ES)+ m/e 581.3 [M+H]⁺.

Example 298 Preparation ofN-{2-(methyloxy)-5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide

a) 7-bromo-2-(1-piperazinyl)quinoxaline

A solution of 7-bromo-2-chloroquinoxaline (20.5 mmol) and piperazine(61.6 mmol) in N,N-dimethylformamide (100 ml) was stirred at 100° C. for18 hours. The reaction was poured into ice-water (200 ml) and extractedwith ethyl acetate (3×100 ml). The combined organic layers were washedwith brine, dried over sodium sulfate, filtered and concentrated invacuo. The product was triturated, filtered, and dried to afford thetitle compound (3.5 g, 58%) as a yellow solid. MS(ES)+ m/e 292.9 [M+H]⁺.

b)7-bromo-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxaline

To a solution of 7-bromo-2-(1-piperazinyl)quinoxaline (3.41 mmol) inpyridine (20 ml) was added 2-(methyloxy)benzenesulfonyl chloride (10.23mmol). The reaction mixture was stirred for 18 hours at 50° C. As thereaction cooled to ambient temperature, a yellow precipitate formedwhich was filtered and the solid triturated with methanol. Theprecipitate was collected to afford the title compound (1.16 g, 73%) asa pale yellow solid. MS(ES)+ m/e 463.0 [M+H]⁺.

c)N-{2-(methyloxy)-5-[3-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}cyclopropanesulfonamide

A slurry of7-bromo-2-(4-{[2-(methyloxy)phenyl]sulfonyl}-1-piperazinyl)quinoxaline(0.54 mmol), bis(pinacolato)diboron (0.81 mmol), potassium acetate (2.15mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.05 mmol) in 1,4-dioxane (4 ml) was heated at 100° C.After the reaction stirred for 1 hour,N-[5-bromo-2-(methyloxy)-3-pyridinyl]cyclopropanesulfonamide (0.81 mmol)and 2M solution potassium carbonate (2 ml) was added and continued tostir for 1 hour. The reaction was cooled to ambient temperature,separated the organic layer and purified directly on silica by columnchromatography (30-100% ethyl acetate/hexanes). The desired fractionswere combined and concentrated to give the title compound (125 mg, 38%yield) as a pale tan solid. MS(ES)+ m/e 611.2 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 298 using the appropriate heteroaryl bromide coupling partnerin step c:

Example Structure MS(ES) [M + H]⁺ 299

585 300

584

Example 301 Preparation ofN,N-dimethyl-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinesulfonamide

a) Phenylmethyl 4-[(dimethylamino)sulfonyl]-1-piperidinecarboxylate

A suspension of an amine such as dimethylamine (4.72 mmol) and sodiumhydride (4.72 mmol) in N,N-dimethylformamide (10 ml) was stirred forfive minutes at room temperature. Then phenylmethyl4-(chlorosulfonyl)-1-piperidinecarboxylate (1.60 mmol) was added to thereaction mixture and stirred at 100° C. for 3 hours. The reactionmixture was poured into water (25 ml) and extracted with ethyl acetate(3×25 ml). The combined organic layers were washed with brine, driedover sodium sulfate, filtered, and concentrated to give the titlecompound (410 mg, 80% yield) as an off-white solid. MS(ES)+ m/e 327.1[M+H]⁺.

b) N,N-dimethyl-4-piperidinesulfonamide

A solution of phenylmethyl4-[(dimethylamino)sulfonyl]-1-piperidinecarboxylate (1.19 mmol) and 10%wt palladium/carbon (0.09 mmol) in methanol (10 ml) was vacuum pumpedand back-filled with nitrogen three times. The nitrogen atmosphere wasthen replaced with hydrogen via a balloon and the reaction stirred for 1hour at ambient temperature. The reaction was then filtered through apad of celite and concentrated to give the title compound (200 mg, 87%yield), which was used directly in the next reaction without furtherpurification. 1H NMR (400 MHz, DMSO-d₆) δ ppm 3.33 (bs, 1H) 3.30-3.22(m, 1H) 2.96 (d, J=12.13, 2H) 2.84 (s, 6H) 2.46 (td, J=2.53, 12.38, 2H)1.80 (d, J=12.13, 2H) 1.46 (qt, J=4.17, 12.34, 2H)

c) 1-(7-bromo-2-quinoxalinyl)-N,N-dimethyl-4-piperidinesulfonamide

A suspension of N,N-dimethyl-4-piperidinesulfonamide (1.03 mmol) andsodium hydride (1.03 mmol) in N,N-dimethylformamide (5 ml) stirred forfive minutes at room temperature. Then 7-bromo-4-chloroquinoxaline (0.86mmol) was added to the reaction mixture and stirred at 100° C. for 3hours. The reaction was poured into water (30 ml) and extracted withethyl acetate (3×25 ml). The combined organic layers were washed withbrine, dried over sodium sulfate, filtered, concentrated, and purifiedon silica by column chromatography to give the title compound (170 mg,50% yield) as yellow solid. MS(ES)+ m/e 399.0 [M+H]⁺.

d)N,N-dimethyl-1-(7-{5-[(phenylsulfonyl)amino]-3-pyridinyl}-2-quinoxalinyl)-4-piperidinesulfonamide

A slurry of1-(7-bromo-2-quinoxalinyl)-N,N-dimethyl-4-piperidinesulfonamide (0.43mmol),N-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide(0.47 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.03 mmol) in 1,4-dioxane (4 ml) and 2M solutionpotassium carbonate (2 ml) was stirred at 100° C. for 18 hours. Thereaction was cooled to ambient temperature, separated the organic layerand purified directly on silica by column chromatography (5%methanol/ethyl acetate). The desired fractions were combined andconcentrated to give the title compound (102 mg, 43% yield) as a yellowsolid. MS(ES)+ m/e 539.2 [M+H]⁺.

The following compounds were or can be prepared following the proceduresin Example 301 using the appropriate amine:

Example Structure MS(ES) [M + H]⁺ 302

539.2 303

525.4 304

569.3

Intermediates Intermediate 1 Preparation of5-bromo-1H-pyrazolo[3,4-b]pyridine

a) 5-bromo-2-fluoro-3-pyridinecarbaldehyde

Following the procedure described in WO2006015124 and trituration of thecrude product in hexanes instead of crystallization from cyclohexaneafforded the title compound as an off-white solid (68%). MS(ES)+ m/e203.8, 205.7 [M+H]⁺.

b) 5-bromo-3-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2(1H)-pyridinonehydrazone

Following the procedure described in WO2006015124 without the additionof hydrogen chloride provided the title compound as a yellow solid.MS(ES)+ m/e 317.9 [M+H]⁺. This crude material was used directly in thenext step.

c) 5-bromo-1H-pyrazolo[3,4-b]pyridine

Following the procedure described in WO2006015124 provided the titlecompound as a yellow solid (94%, 2 steps). MS(ES)+ m/e 197.7, 199.7[M+H]⁺.

Intermediate 2 Preparation of2-amino-5-bromo-N,N-dimethyl-3-pyridinesulfonamide

a) 2-amino-5-bromo-3-pyridinesulfonyl chloride

To a cooled (0° C.) solution of chlorosulfonic acid (58 mL) undervigorous stirring was added 5-bromo-2-pyridinamine (86.7 mmol)portionwise. The reaction mixture was then heated at reflux for 3 hrs.Upon cooling to room temperature, the reaction mixture was poured overice (˜100 g) with vigorous stirring. The resulting yellow precipitatewas collected by suction filtration, washing with cold water andpetroleum ether to provide the title compound as an orange-yellow solid(18.1 g, 77% yield). MS(ES)+ m/e 272.8 [M+H]⁺.

* Other sulfonyl chlorides can be prepared using this procedure byvarying the choice of substituted aryl or heteroaryl.

b) 2-amino-5-bromo-N,N-dimethyl-3-pyridinesulfonamide

To a cold (0 □C) suspension of 2-amino-5-bromo-3-pyridinesulfonylchloride (92.1 mmol) in dry 1,4-dioxane (92 mL) was added pyridine(101.3 mmol) followed by a 2M solution of dimethylamine in THF (101.3mmol). The reaction was allowed to warm to rt for 2 h, heated to 50 □Cfor 1 h, then cooled to rt. After standing for 2 h, the precipitate wascollected by filtration and rinsed with a minimal amount of cold water.Drying the precipitate to constant weight under high vacuum provided14.1 g (55%) of the title compound as a white solid. MS(ES)+ m/e 279.8,282.0 [M+H]⁺.

*Other sulfonamides were or can be prepared using this procedure byvarying the choice of starting sulfonyl chloride and amine.

Intermediate 3 Preparation of2-amino-N,N-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinesulfonamide

To a solution of 2-amino-5-bromo-N,N-dimethyl-3-pyridinesulfonamide(7.14 mmol) in 1,4-dioxane (35 mL) was added4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi-1,3,2-dioxaborolane (7.86 mmol),potassium acetate (28.56 mmol) and[1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.571 mmol). The reaction mixture was stirred at 100° C.for 18 h. The reaction was concentrated in vacuo, re-dissolved in ethylacetate (50 mL) and purified on silica using 60% ethyl acetate/hexanesto yield the title compound as a tan solid (86%). 1H NMR (400 MHz,DMSO-d₆) δ ppm 8.41 (d, 1H, J=1.52), 7.92 (d, 1H, J=1.77), 2.68 (s, 6H),1.28 (s, 12H).

* Other boronate or boronic acids can be prepared using this procedureby varying the choice of starting aryl or heteroaryl bromide.

Intermediate 4 Preparation ofN-(5-bromo-2-chloro-3-pyridinyl)benzenesulfonamide

To a stirred solution of a pyridineamine such as3-amino-5-bromo-2-chloropyridine (24 mmol) in dichloromethane (50 mL)was added pyridine (37 mmol) followed by benzenesulfonyl chloride (35mmol) dropwise over 5 minutes. The reaction mixture was stirred at RTfor 18 h and evaporated to dryness in vacuo. The residue was purified byflash chromatography on silica gel (15% hexanes in CH₂Cl₂ then 0 to 5%EtOAc in 15% hexanes in CH₂Cl₂). During evaporation of the solvents theproduct crashed out. The resultant slurry was diluted with hexanes,filtered and dried under vacuum to give the title compound (2.89 g, 34%)as a white solid. MS (ES) m/e 346.7 (M+H)⁺.

* Other pyridinesulfonamides were or can be prepared using thisprocedure by varying the choice of starting pyridineamine andsulfonylchloride.

Intermediate 5 Preparation ofN-[5-bromo-2-(methyloxy)-3-pyridinyl]-1-ethyl-1H-pyrazole-4-sulfonamide

In an oven dried round bottom flask under a nitrogen atmosphere, asolution of 5-bromo-2-(methyloxy)-3-pyridinamine (268 mg, 1.320 mmol) inanhydrous pyridine (4 mL) was treated with1-ethyl-1H-pyrazole-4-sulfonyl chloride (308 mg, 1.584 mmol) and theresultant reaction mixture stirred at room temperature for 90 min. Thereaction mixture was concentrated in vacuo, diluted with ethyl acetate(100 mL) and water (30 mL), neutralized with saturated ammonium chloride(aq) and the product extracted into the organic layer. The aqueous layerwas back-extracted with 40 mL ethyl acetate. The organic layers werecombined, washed with brine (50 mL), dried over magnesium sulfate andconcentrated in vacuo to give a yellow-brown solid. Purification bysilica gel chromatography (0-50% ethyl acetate in hexanes) provided thetitle compound (368 mg, 77%) as a beige solid. MS(ES)+ m/e 361.0, 363.0[M+H]⁺.

* Related aryl-aminosulfonylpyridinyl bromides were or can be preparedusing this procedure by varying the choice of starting pyridineamine andsulfonyl chloride.

Intermediate 6 Preparation ofN-[5-bromo-2-(methyloxy)-3-pyridinyl]cyclopropanesulfonamide

A solution of 5-bromo-2-(methyloxy)-3-pyridinamine (1.65 g, 8.13 mmol)in anhydrous pyridine (20 ml) was treated with neat cyclopropanesulfonylchloride (1.371 g, 9.75 mmol) then stirred at room temperature for 20 h.The resulting slurry was concentrated under reduced pressure to aresidue that was purified by column chromatography on silica, elutingwith 30% hexanes in dichloromethane. The combined desired fractions wereconcentrated under reduced pressure to give the title compound (1.61 g,60%) as an off white solid. MS(ES)+ m/e 306.9, 309.0 [M+H]⁺.

* Related alkyl-aminosulfonylpyridinyl bromides were or can be preparedusing this procedure by varying the choice of starting pyridineamine andsulfonyl chloride.

Intermediate 7 Preparation ofN-(5-bromo-2-methyl-3-pyridinyl)cyclopropanesulfonamide a)5-bromo-2-methyl-3-nitropyridine

Sodium hydride (1.31 g, 54.8 mmol, 2.19 g of 60% in mineral oil) wassuspended in dry THF (70 mL) and to this suspension was added5-bromo-2-chloro-3-nitropyridine as a solid. An ambient water bath wasplaced under the reaction and a solution of diethyl malonate in dry THF(15 mL) was added carefully via addition funnel. Observed a vigorousevolution of gas. After 2 hours additional sodium hydride (0.202 g, 8.42mmol, 0.337 g of 60% in mineral oil) was added and the reaction wasstirred for 1.5 hours. The reaction was concentrated in vacuo, dilutedwith 6N HCl (100 ml), and refluxed overnight. The reaction wasconcentrated in vacuo and diluted with saturated sodium carbonate to pH9. The basic aqueous mixture was diluted with dichloromethane andfiltered through filter paper to remove an insoluble green solid. Thefiltrate was transferred to a separatory funnel and the layers wereseparated. The dichloromethane was washed with saturated sodium chloride(aq), dried over sodium sulfate, filtered and concentrated to give thetitle compound (5.79 g, 63.3%) as an orange oil. MS(ES)⁺ m/e 217 [M+H].

b) 5-bromo-2-methyl-3-pyridinamine

A mixture of 5-bromo-2-methyl-3-nitropyridine (5.68 g, 26.2 mmol) andtin(II)chloride dihydrate in ethyl acetate (200 mL) was refluxed for 2hours and concentrated in vacuo. The residue was diluted with 6N NaOH(200 mL), water (100 mL), and dichloromethane (300 mL) and stirred atroom temperature. The mixture was filtered through filter paper toremove small amounts of undissolved solid and the biphasic mixture wastransferred to a separatory funnel. The layers were separated and theorganic layer was washed with saturated NaCl, dried over Na₂SO₄,filtered and concentrated to give a gummy orange solid. The solid wastriturated with warm hexanes, filtered, and dried in a Buchner funnel togive the title compound (3.03 g, 62%) as a tan solid. MS(ES)⁺ m/e 375[2M+H].

c) N-(5-bromo-2-methyl-3-pyridinyl)cyclopropanesulfonamide

In an oven dried round bottom flask under nitrogen, a solution of5-bromo-2-methyl-3-pyridinamine (150 mg, 0.802 mmol) in anhydrouspyridine (4 mL) was treated with cyclopropanesulfonyl chloride (0.098mL, 0.962 mmol) and the resultant reaction mixture stirred at roomtemperature for 18.75 hours. The reaction mixture was concentrated invacuo, diluted with ethyl acetate (100 mL) and water (30 mL),neutralized with saturated ammonium chloride (aq) and the productextracted into the organic layer. The aqueous layer was back-extractedwith ethyl acetate (40 mL) and the combined organic layers washed withbrine (50 mL), dried over magnesium sulfate, filtered and concentratedin vacuo to give a yellow-brown solid. Purification by silica gelchromatography (0-50% ethyl acetate in hexanes) provided the titlecompound (218 mg, 93%) as an off-white solid. MS(ES)+ m/e 290.9, 292.8[M+H]⁺.

* Related alkyl, aryl, or heteroaryl-aminosulfonylpyridinyl bromides canbe prepared using this procedure by varying the choice of sulfonylchloride.

Intermediate 8 Preparation ofN-(5-bromo-3-pyridinyl)cyclopropanesulfonamide

In a 20 ml vial was combined 5-bromo-3-pyridinamine (7.5 g, 43.3 mmol)and cyclopropanesulfonyl chloride (9.14 g, 65.0 mmol), dioxane (6 mL)and pyridine (3 mL) to give a brown suspension. The reaction mixture wassealed and stirred at 50° C. for 24 h. LCMS showed product and 5%starting material. The reaction mixture was diluted with dichloromethaneand washed with saturated sodium bicarbonate (aq). The organic layer wasconcentrated in vacuo and the residue was precipitated with water.Filtration and washing of the solid with water followed by hexanesprovided the desired product as a brown solid (9.6 g, 80% yield). ESMSm/e: 276.8, 278.8 [M]⁺.

* Related alkyl-aminosulfonylpyridinyl bromides were or can be preparedusing this procedure by varying the choice of sulfonyl chloride.

Intermediate 9 Preparation of N-(5-bromo-3-pyridinyl)benzenesulfonamide

In a 500 mL round-bottomed flask was combined 5-bromo-3-pyridinamine (30g, 173 mmol), triethylamine (53.2 mL, 381 mmol) and dichloromethane (150mL). The reaction mixture was cooled to 0° C. and benzenesulfonylchloride (48.9 mL, 381 mmol) was added slowly to give a brown solution.The reaction mixture was stirred for 1 h at room temperature, giving 77%bis-sulfonylated product, MW=454.8 and 17% desired mono-sulfonylatedproduct, MW=312.9. The reaction mixture was concentrated in vacuo, theresidue titrated with methanol and the solid filtered to yield a whitesolid.

This solid was suspended in a 1:1 methanol:6N sodium hydroxide (aq)solution and allowed to stir for 3 h at RT. LCMS showed 84% desiredmono-sulfonylated product. The reaction mixture was concentrated invacuo and neutralized with 6N HCl (aq). The precipitate that formed wasfiltered and dried to an off-white solid. The solid was titrated withMeOH, filtered, and dried to give clean desired product as an off-whitesolid (99% yield). ESMS m/e 315.0 [M+H]⁺.

-   -   Related aryl- or heteroaryl-aminosulfonylpyridinyl bromides can        be prepared using this procedure by varying the choice of        sulfonyl chloride.

Intermediate 10 Preparation ofN-(5-bromo-3-pyridinyl)-2,4-difluorobenzenesulfonamide

A solution of 5-bromo-3-pyridinamine (104 mmol) in dichloromethane (55mL) was added dropwise over ˜60 min to a stirred solution oftriethylamine (230 mmol) and 2,4-difluorobenzenesulfonyl chloride (235mmol) in dichloromethane (300 mL). After 1.5 h, additional2,4-difluorobenzenesulfonyl chloride (53.4 mmol) was added, and after 2days, more 2,4-difluorobenzenesulfonyl chloride (47.0 mmol) andtriethylamine (108 mmol) were added. After 1 h, the resulting mixture ofmono- and bis-sulfonylation products was concentrated in vacuo and theresidue was suspended in methanol (500 mL) and then filtered to provideN-(5-bromo-3-pyridinyl)-N-[(2,4-difluorophenyl)sulfonyl]-2,4-difluorobenzenesulfonamideas a white solid (54.4 mmol, 52%).

A solution of the bis-sulfonylated intermediate (54.4 mmol) in1,4-dioxane (300 mL) was heated to 80° C. A solution of potassiumhydroxide (322 mmol) in water (133 mL) was added and the resultantreaction mixture was heated at reflux for 0.5 h. The dioxane was removedin vacuo and the resulting off-white suspension was acidified withconcentrated HCl, causing the solids to dissolve and then a newoff-white solid to emerge. The suspension was stirred for 30 min andthen filtered, rinsing with water. The solid was dried in vacuo and thendesiccated over P₂O₅ to afford the title product as an off-white solid(quantitative yield). ESMS m/e 347, 349 [M+H]⁺.

Intermediate 11 Preparation ofN-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]benzenesulfonamide

N-(5-bromo-3-pyridinyl)benzenesulfonamide (25 g, 80 mmol),4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi-1,3,2-dioxaborolane (24.33 g, 96mmol), PdCl₂(dppf).CH₂Cl₂ (2.61 g, 3.19 mmol), and potassium acetate(31.3 g, 319 mmol) were added to a 500 mL round bottom flask equippedwith an oven-dried stir bar and a reflux condensor under a nitrogenatmosphere. 1,4-Dioxane (400 ml) was added and the reaction mixturestirred at 100° C. for 18 h. LCMS showed complete conversion to desiredproduct (89% boronic acid by LCMS, M+H=278.9). The reaction mixture wascooled to room temperature and then concentrated in vacuo to a blackresidue. The residue was suspended in water (250 mL) and extracted withethyl acetate (4×150 mL). The combined black organic layers were driedover sodium sulfate and decolorizing carbon, filtered through a pad ofcelite and concentrated to yield an orange solid. The solid was titratedwith dichloromethane, collected by suction filtration and dried in vacuoto yield a white solid (61% yield). ESMS m/e: 278.9 (boronic acid)[M+H]⁺.

* Related aryl- or heteroaryl-aminosulfonylpyridinyl boronate esters canbe prepared using this procedure by varying the choice of starting aryl-or heteroaryl-aminosulfonylpyridinyl bromides.

Intermediate 12 Preparation ofN′-(5-bromo-3-pyridinyl)-N,N-dimethylsulfamide

In an oven-dried flask under nitrogen, dimethylsulfamoyl chloride (0.310mL, 2.89 mmol) was added by syringe to a solution of3-amino-5-bromopyridine (500 mg, 2.89 mmol) and pyridine (0.467 mL, 5.78mmol) in dichloromethane (10 mL) at room temperature. The reaction wasstirred for 4 hours and then added additional dimethylsulfamoyl chloride(0.310 mL, 2.89 mmol) to the reaction and stirred overnight (20 hours).The reaction was concentrated in vacuo. The residue was taken up into200 mL ethyl acetate and washed with saturated aqueous sodiumbicarbonate solution (100 mL) followed by brine (100 mL). The organiclayer was dried over magnesium sulfate and concentrated in vacuo to givethe title compound (839 mg, 93%) as a brown solid. MS(ES)+ m/e 279.9,282.0 [M+H]⁺.

* Related sulfamides can be prepared using this procedure by varying thechoice of starting pyridineamine bromides and sulfamoyl chlorides.

Intermediate 13 Preparation of 7-bromo-2-(1H-pyrazol-4-yl)quinoxaline

To a 100 mL high pressure vessel was added 1,1-dimethylethyl4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate(1.208 g, 4.11 mmol), 7-bromo-2-chloroquinoxaline (1 g, 4.11 mmol),PdCl₂(dppf).CH₂Cl₂ (0.168 g, 0.205 mmol), 1,4-dioxane (20.53 ml) and 2Maqueous potassium carbonate (10.27 ml, 20.53 mmol). The vessel wassealed and the reaction mixture heated at 100° C. overnight (21.5 hrs).LCMS showed 60% desired product (M+H=276.9) with no Boc group. Theorganic layer was separated and purified directly on a silica gelcolumn, eluting with 50% ethyl acetate to 100% ethyl acetate in hexanes.The desired fractions were concentrated in vacuo to give a tan solidwhich was triturated with ethyl acetate, the insolubles collected bysuction filtration and dried in vacuo to provide the title compound as atan powder (508 mg, 45%). ESMS m/e 276.9 [M+H]⁺.

Intermediate 14 Preparation of2-[4-(7-bromo-2-quinoxalinyl)-1H-pyrazol-1-yl]-N,N-dimethylethanamine

To a solution of 7-bromo-2-(1H-pyrazol-4-yl)quinoxaline (0.225 g, 0.808mmol) in dry N,N-dimethylformamide (5 mL) under a nitrogen atmospherewas added 60 wt % sodium hydride (92 mg, 2.27 mmol) portionwise. After 5minutes of stirring with purging, 2-dimethylaminoethylbromide (0.37 g,0.908 mmol) was added and the reaction mixture stirred at rt for 30 min,concentrated in vacuo and taken into dichloromethane. The organicsolution was washed with water (2×), dried (Na₂SO₄), filtered andconcentrated in vacuo. The residue was purified by silica gelchromatography, eluting with 0-5% methanol in ethyl acetate to furnishthe title compound (0.183 g, 66% yield). ESMS m/e: 345.9; 347.8 [M]⁺.

* Related alkylated, acylated and sulfonylated pyrazoles were or can beprepared using this procedure by varying the choice of alkylbromide,acyl chloride or sulfonyl chloride.

Intermediate 15 Preparation of7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxaline

A slurry of 7-bromo-2-chloroquinoxaline (10.0 mmol),1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole(10.5 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethanecomplex (1:1) (0.3 mmol) in 2M aqueous potassium carbonate (15 mL) and1,4-dioxane (40 mL) was heated at 100° C. for 4 h. The reaction mixturewas cooled, poured into water (100 mL), and extracted with (3×100 mL)ethyl acetate. The combined organic layers were filtered through a padof Celite while rinsing with water and ethyl acetate. The filtrate wasseparated and the organic layer was dried over sodium sulfate, filtered,and concentrated in vacuo. Purification of the residue by silica gelchromatography (40-70% ethyl acetate/hexanes) provided the titlecompound as a yellow solid (1.73 g, 57%). MS(ES)+ m/e 289, 291 [M+H]⁺.

* Related aryl or heteroaryl substituted quinoxalines can be preparedusing this procedure by varying the choice of aryl- or heteroarylboronic acid or boronate ester.

Intermediate 16 Preparation of2-(1-methyl-1H-pyrazol-4-yl)-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline

In a 100 mL roundbottom flask, a mixture of7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxaline (10.03 mmol),bis(pinacolato)diboron (12.21 mmol), potassium acetate (32.6 mmol), and[1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethane complex (1:1) (0.465 mmol) in dioxane (68 mL) wasstirred at 100° C. for 18 h.

The reaction mixture was filtered, washing with 100 mL ethyl acetate.The filtrate was concentrated in vacuo and the brown residue dissolvedin hot ethyl acetate (˜20 mL). The dark solution was filtered and thefiltrate concentrated in vacuo. The residue was partitioned betweenethyl acetate (100 mL) and water (70 mL) and the organic phaseseparated, dried over magnesium sulfate, filtered and concentrated to˜10 mL, then treated with portions of hexanes (˜2 volumes). A fine, darksolid precipitate formed which was removed by filtration, and thefiltrate was evaporated to an olive residue. The residue was trituratedwith 3:1 hexanes/ethyl acetate (40 mL) and the resulting light olivegreen solid collected and dried in vacuo to provide the title compound(2.2 g, 59%). MS(ES)+ m/e 337.2, 339.2 [M+H]⁺.

Intermediate 17 Preparation of N,N-dimethyl-4-piperidinesulfonamide

a) phenylmethyl 4-[(dimethylamino)sulfonyl]-1-piperidinecarboxylate

A suspension of an amine such as dimethylamine (4.72 mmol) and sodiumhydride (4.72 mmol) in N,N-dimethylformamide (10 ml) was stirred forfive minutes at room temperature. Then phenylmethyl4-(chlorosulfonyl)-1-piperidinecarboxylate (1.60 mmol) was added to thereaction mixture and stirred at 100° C. for 3 hours. The reactionmixture was poured into water (25 ml) and extracted with ethyl acetate(3×25 ml). The combined organic layers were washed with brine, driedover sodium sulfate, filtered, and concentrated to give the titlecompound (410 mg, 80% yield) as an off-white solid. MS(ES)+ m/e 327.1[M+H]⁺.

b) N,N-dimethyl-4-piperidinesulfonamide

A solution of phenylmethyl4-[(dimethylamino)sulfonyl]-1-piperidinecarboxylate (1.19 mmol) and 10%wt palladium/carbon (0.09 mmol) in methanol (10 ml) was vacuum pumpedand back-filled with nitrogen three times. The nitrogen atmosphere wasthen replaced with hydrogen via a balloon and the reaction stirred for 1hour at ambient temperature. The reaction was then filtered through apad of celite and concentrated to give the title compound (200 mg, 87%yield), which was used directly in the next reaction without furtherpurification. 1H NMR (400 MHz, DMSO-d₆) δ ppm 3.33 (bs, 1H) 3.30-3.22(m, 1H) 2.96 (d, J=12.13, 2H) 2.84 (s, 6H) 2.46 (td, J=2.53, 12.38, 2H)1.80 (d, J=12.13, 2H) 1.46 (qt, J=4.17, 12.34, 2H)

* Related piperidinylsulfonamides can be prepared using this procedureby varying the choice of amine.

Other Intermediates can be Prepared Following the General Scheme Below:

Exemplary Capsule Composition

An oral dosage form for administering the present invention is producedby filing a standard two piece hard gelatin capsule with the ingredientsin the proportions shown in Table II, below.

TABLE II INGREDIENTS AMOUNTS Compound of example 1 25 mg Lactose 55 mgTalc 16 mg Magnesium Stearate  4 mg

Exemplary Injectable Parenteral Composition

An injectable form for administering the present invention is producedby stirring 1.5% by weight of compound of example 1 in 10% by volumepropylene glycol in water.

Exemplary Tablet Composition

The sucrose, calcium sulfate dihydrate and an PI3K inhibitor as shown inTable III below, are mixed and granulated in the proportions shown witha 10% gelatin solution. The wet granules are screened, dried, mixed withthe starch, talc and stearic acid, screened and compressed into atablet.

TABLE III INGREDIENTS AMOUNTS Compound of example 1 20 mg calciumsulfate dehydrate 30 mg Sucrose 4 mg Starch 2 mg Talc 1 mg stearic acid0.5 mg

While the preferred embodiments of the invention are illustrated by theabove, it is to be understood that the invention is not limited to theprecise instructions herein disclosed and that the right to allmodifications coming within the scope of the following claims isreserved.

1. A compound of Formula (I):

in which R1 is an optionally substituted ring system selected from agroup consisting of: formula (II), (III), (IV), (V), (VI), (VII) and(VIII):

each R2, R3 and R4 is independently selected from: hydrogen, halogen,acyl, amino, substituted amino, arylamino, acylamino,heterocycloalkylamino, C1-6alkyl, substituted C1-6alkyl, C3-7cycloalkyl,substituted C3-7cycloalkyl, C3-7heterocycloalkyl, substitutedC3-7heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl, substituted aryl,heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl,arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl, substitutedheteroarylalkyl, cyano, hydroxyl, alkoxy, acyloxy, and aryloxy; n is0-2; X is C or N; Y is C, O, N, or S; and/or a pharmaceuticallyacceptable salt thereof; provided that in each of formula (V) to (VIII)at least one Y is not carbon; further provided that formula (VIII) issubstituted with at least one oxo group; further provided that R1 is notimidazolidinedione, and when R1 is 4-pyridinyl R2 is not substitutedaryl, thienyl or substituted thienyl.
 2. A compound according to claim1, wherein R1 is selected from a group consisting of: formula (II),(III) and (IV); or a pharmaceutically acceptable salt thereof.
 3. Acompound according to claim 1, wherein R1 is an optionally substitutedsix-membered heteroaryl ring containing at least one nitrogen.
 4. Acompound according to claim 1, wherein R1 is selected from a groupconsisting of: formula (V) and (VI), wherein Y is C or N; or apharmaceutically acceptable salt thereof.
 5. A compound according toclaim 1, wherein R1 is selected from a group consisting of: formula(VII) and (VIII); or a pharmaceutically acceptable salt thereof.
 6. Acompound according to claim 1, wherein R1 is an optionally substitutedpyridinyl ring.
 7. A compound according to claim 1, wherein R3 and R4are hydrogens, and R2 is selected from a group consisting of: aryl,heteroaryl, substituted aryl, substituted heteroaryl, heterocycloalkyl,substituted heterocycloalkyl, amino, substituted amino, arylamino,acylamino, heterocycloalkylamino, hydroxyl, alkoxy, C1-6alkyl andsubstituted C1-6alkyl; or a pharmaceutically acceptable salt thereof;provided that R2 is not thienyl or substituted thienyl.
 8. A compound ofFormula (I)(G):

in which each R2, R3, R4 and R5 is independently selected from:hydrogen, halogen, acyl, amino, substituted amino, arylamino, acylamino,heterocycloalkylamino, C1-6alkyl, substituted C1-6alkyl, C3-7cycloalkyl,substituted C3-7cycloalkyl, C3-7heterocycloalkyl, substitutedC3-7heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl, substituted aryl,heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl,arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl, substitutedheteroarylalkyl, cyano, hydroxyl, alkoxy, acyloxy, and aryloxy; or R5 isR6, wherein R6 is —SO2NR80 or —NSO₂R80, in which R80 is selected from agroup consisting of: C1-C6alkyl, C1-C6cycloalkyl, C1-C6heterocycloalkyl,substituted C1-C6alkyl, substituted C1-C6cycloalkyl, substitutedC1-C6heterocycloalkyl, aryl optionally fused with a five-membered ringor substituted with one to five groups selected from a group consistingof: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH, orheteroaryl optionally fused with a five-membered ring or substitutedwith one to five groups selected from a group consisting of: C1-C6alkyl,C1-C6cycloalkyl, halogen, amino, trifluoromethyl, cyano, hydroxyl,alkoxy, oxo, or —(CH₂)_(n)COOH; n is 0-2, m is 0-2; or apharmaceutically acceptable salt thereof; provided that R2 is notthienyl or substituted thienyl.
 9. A compound of Formula (I)(H)according to claim 8:

in which R2 is selected from a group consisting of: heteroaryl,substituted heteroaryl, heterocycloalkyl, substituted heterocycloalkyl,amino, substituted amino, arylamino, acylamino, heterocycloalkylamino,alkoxy, C1-6alkyl and substituted C1-6alkyl; each R3 and R4 isindependently selected from: hydrogen, halogen, acyl, amino, substitutedamino, C1-6alkyl, substituted C1-6alkyl, C3-7cycloalkyl, substitutedC3-7cycloalkyl, C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl,cyano, hydroxyl and alkoxy; each R5 is independently selected from:hydrogen, halogen, acyl, amino, substituted amino, C1-6alkyl,substituted C1-6alkyl, C3-7cycloalkyl, substituted C3-7cycloalkyl,C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl, cyano, hydroxyl,alkoxy, nitro; or R5 is R6, wherein R6 is —SO2NR80 or —NSO₂R80, in whichR80 is selected from a group consisting of: C1-C6alkyl, C1-C6cycloalkyl,C1-C6heterocycloalkyl, substituted C1-C6alkyl, substitutedC1-C6cycloalkyl, substituted C1-C6heterocycloalkyl, aryl optionallyfused with a five-membered ring or substituted with one to five groupsselected from a group consisting of: C1-C6alkyl, C1-C6cycloalkyl,halogen, amino, substituted amino, trifluoromethyl, cyano, hydroxyl,alkoxy, oxo or —(CH₂)_(n)COOH, or heteroaryl optionally fused with afive-membered ring or substituted with one to five groups selected froma group consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or —(CH₂)_(n)COOH; n is0-2, m is 0-2; or a pharmaceutically acceptable salt thereof; providedthat R2 is not thienyl or substituted thienyl.
 10. A compound of Formula(I)(J) according to claim 8:

in which R2 is selected from a group consisting of: heteroaryl,substituted heteroaryl, heterocycloalkyl, substituted heterocycloalkyl,amino, substituted amino, arylamino, acylamino, heterocycloalkylamino,alkoxy, C1-6alkyl and substituted C1-6alkyl; each R3 and R4 isindependently selected from: hydrogen, halogen, acyl, amino, substitutedamino, C1-6alkyl, substituted C1-6alkyl, C3-7cycloalkyl, substitutedC3-7cycloalkyl, C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl,cyano, hydroxyl and alkoxy; each R5 is independently selected from:hydrogen, halogen, acyl, amino, substituted amino, C1-6alkyl,substituted C1-6alkyl, C3-7cycloalkyl, substituted C3-7cycloalkyl,C3-7heterocycloalkyl, substituted C3-7heterocycloalkyl, cyano, hydroxyl,alkoxy, nitro; R6 is —SO2NR80 or —NSO₂R80, in which R80 is selected froma group consisting of: C1-C6alkyl, C1-C6cycloalkyl,C1-C6heterocycloalkyl, substituted C1-C6alkyl, substitutedC1-C6cycloalkyl, substituted C1-C6heterocycloalkyl, aryl optionallyfused with a five-membered ring or substituted with one to five groupsselected from a group consisting of: C1-C6alkyl, C1-C6cycloalkyl,halogen, amino, substituted amino, trifluoromethyl, cyano, hydroxyl,alkoxy, oxo or —(CH₂)_(n)COOH, or heteroaryl optionally fused with afive-membered ring or substituted with one to five groups selected froma group consisting of: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino,trifluoromethyl, cyano, hydroxyl, alkoxy, oxo, or —(CH₂)_(n)COOH; n is0-2, m is 0-2; or a pharmaceutically acceptable salt thereof.
 11. Acompound of Formula (I)(M) according to claim 8:

in which R2 is selected from a group consisting of: heteroaryl,substituted heteroaryl, heterocycloalkyl, substituted heterocycloalkyl,amino, substituted amino, arylamino, acylamino, heterocycloalkylaminoalkoxy, C1-6alkyl and substituted C1-6alkyl; each R5 is independentlyselected from: hydrogen, halogen, acyl, amino, substituted amino,C1-6alkyl, substituted C1-6alkyl, cyano, hydroxyl, alkoxy; m is 0-1; R6is —NSO₂R80, wherein R80 is selected from a group consisting of:C1-C6alkyl, C1-C6cycloalkyl, C1-C6heterocycloalkyl, substitutedC1-C6alkyl, substituted C1-C6cycloalkyl, substitutedC1-C6heterocycloalkyl, aryl optionally fused with a five-membered ringor substituted with one to five groups selected from a group consistingof: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH, orheteroaryl optionally fused with a five-membered ring or substitutedwith one to five groups selected from a group consisting of: C1-C6alkyl,C1-C6cycloalkyl, halogen, amino, trifluoromethyl, cyano, hydroxyl,alkoxy, oxo, or —(CH₂)_(n)COOH, n is 0-2.
 12. A compound of Formula(I)(N) according to claim 8:

in which R2 is selected from a group consisting of: heteroaryl,substituted heteroaryl, heterocycloalkyl, substituted heterocycloalkyl,amino, substituted amino, arylamino, acylamino, heterocycloalkylaminoalkoxy, C1-6alkyl and substituted C1-6alkyl; each R5 is independentlyselected from: hydrogen, halogen, acyl, amino, substituted amino,C1-6alkyl, substituted C1-6alkyl, cyano, hydroxyl, alkoxy; m is 0-1; R6is —SO2NR80, wherein R80 is selected from a group consisting of:C1-C6alkyl, C1-C6cycloalkyl, C1-C6heterocycloalkyl, substitutedC1-C6alkyl, substituted C1-C6cycloalkyl, substitutedC1-C6heterocycloalkyl, aryl optionally fused with a five-membered ringor substituted with one to five groups selected from a group consistingof: C1-C6alkyl, C1-C6cycloalkyl, halogen, amino, substituted amino,trifluoromethyl, cyano, hydroxyl, alkoxy, oxo or —(CH₂)_(n)COOH, orheteroaryl optionally fused with a five-membered ring or substitutedwith one to five groups selected from a group consisting of: C1-C6alkyl,C1-C6cycloalkyl, halogen, amino, trifluoromethyl, cyano, hydroxyl,alkoxy, oxo, or —(CH₂)_(n)COOH, n is 0-2.
 13. A pharmaceuticalcomposition comprising a compound according to claim 1 and apharmaceutically acceptable carrier.
 14. A method of inhibiting one ormore phosphatoinositides 3-kinases (PI3Ks) in a human; comprisingadministering to the mammal a therapeutically effective amount of acompound of Formula (I) or a pharmaceutically acceptable thereof asdefined in claim
 1. 15. A method of treating one or more disease statesselected from a group consisting of: autoimmune disorders, inflammatorydiseases, cardiovascular diseases, neurodegenerative diseases, allergy,asthma, pancreatitis, multiorgan failure, kidney diseases, plateletaggregation, cancer, sperm motility, transplantation rejection, graftrejection and lung injuries, in a human, which method comprisesadministering to a human in need thereof, a therapeutically effectiveamount of a compound according to claim
 1. 16. A method of treatingcancer comprises co-administration a compound according to claim 1; or apharmaceutically acceptable salt, hydrate, solvate or pro-drug thereof;and at least one anti-neoplastic agent, such as one selected from agroup consisting of anti-microtubule agents, platinum coordinationcomplexes, alkylating agents, antibiotic agents, topoisomerase IIinhibitors, antimetabolites, topoisomerase I inhibitors, hormones andhormonal analogues, signal transduction pathway inhibitors, non-receptortyrosine kinase angiogenesis inhibitors, immunotherapeutic agents,proapoptotic agents, and cell cycle signaling inhibitors.
 17. A methodof claim 10 wherein the disease is cancer.
 18. A method of claim 16wherein the cancer is selected from a group consisting of: brain(gliomas), glioblastomas, leukemias, Bannayan-Zonana syndrome, Cowdendisease, Lhermitte-Duclos disease, breast, inflammatory breast cancer,Wilm's tumor, Ewing's sarcoma, Rhabdomyosarcoma, ependymoma,medulloblastoma, colon, head and neck, kidney, lung, liver, melanoma,ovarian, pancreatic, prostate, sarcoma, osteosarcoma, giant cell tumorof bone and thyroid,
 19. A method of claim 16 wherein the disease isselected from a group consisting of: ovarian cancer, pancreatic cancer,breast cancer, prostate cancer and leukemia.
 20. A method of claim 9,wherein said PI3 kinase is a PI3α.
 21. A method of claim 9 wherein thecompound according to claim 1, or a pharmaceutically acceptable salt, isadministered in a pharmaceutical composition.